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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs4774585

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr15:51324283 (GRCh38.p14) Help

The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.

Alleles
G>A
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.196607 (52040/264690, TOPMED)
A=0.214031 (33498/156510, ALFA)
A=0.186382 (26124/140164, GnomAD) (+ 19 more)
A=0.17675 (13910/78700, PAGE_STUDY)
A=0.00563 (159/28258, 14KJPN)
A=0.00555 (93/16760, 8.3KJPN)
A=0.1626 (1041/6404, 1000G_30x)
A=0.1603 (803/5008, 1000G)
A=0.1636 (733/4480, Estonian)
A=0.2117 (816/3854, ALSPAC)
A=0.2260 (838/3708, TWINSUK)
A=0.0120 (35/2922, KOREAN)
A=0.1845 (530/2872, PharmGKB)
A=0.1339 (253/1890, HapMap)
A=0.0120 (22/1832, Korea1K)
A=0.196 (196/998, GoNL)
A=0.185 (111/600, NorthernSweden)
A=0.130 (28/216, Qatari)
A=0.024 (5/212, Vietnamese)
G=0.449 (61/136, SGDP_PRJ)
A=0.28 (11/40, GENOME_DK)
G=0.44 (8/18, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
CYP19A1 : Intron Variant
Publications
3 citations
Genomic View
See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315
Population Group Sample Size Ref Allele Alt Allele
Total Global 156604 G=0.785995 A=0.214005
European Sub 134940 G=0.785305 A=0.214695
African Sub 7110 G=0.8451 A=0.1549
African Others Sub 242 G=0.864 A=0.136
African American Sub 6868 G=0.8445 A=0.1555
Asian Sub 664 G=0.986 A=0.014
East Asian Sub 532 G=0.987 A=0.013
Other Asian Sub 132 G=0.985 A=0.015
Latin American 1 Sub 752 G=0.816 A=0.184
Latin American 2 Sub 6330 G=0.7060 A=0.2940
South Asian Sub 190 G=0.768 A=0.232
Other Sub 6618 G=0.7900 A=0.2100


Help

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download
Study Population Group Sample Size Ref Allele Alt Allele
TopMed Global Study-wide 264690 G=0.803393 A=0.196607
Allele Frequency Aggregator Total Global 156510 G=0.785969 A=0.214031
Allele Frequency Aggregator European Sub 134864 G=0.785287 A=0.214713
Allele Frequency Aggregator African Sub 7110 G=0.8451 A=0.1549
Allele Frequency Aggregator Other Sub 6600 G=0.7897 A=0.2103
Allele Frequency Aggregator Latin American 2 Sub 6330 G=0.7060 A=0.2940
Allele Frequency Aggregator Latin American 1 Sub 752 G=0.816 A=0.184
Allele Frequency Aggregator Asian Sub 664 G=0.986 A=0.014
Allele Frequency Aggregator South Asian Sub 190 G=0.768 A=0.232
gnomAD - Genomes Global Study-wide 140164 G=0.813618 A=0.186382
gnomAD - Genomes European Sub 75898 G=0.80297 A=0.19703
gnomAD - Genomes African Sub 41998 G=0.84983 A=0.15017
gnomAD - Genomes American Sub 13660 G=0.73521 A=0.26479
gnomAD - Genomes Ashkenazi Jewish Sub 3324 G=0.7641 A=0.2359
gnomAD - Genomes East Asian Sub 3130 G=0.9840 A=0.0160
gnomAD - Genomes Other Sub 2154 G=0.8087 A=0.1913
The PAGE Study Global Study-wide 78700 G=0.82325 A=0.17675
The PAGE Study AfricanAmerican Sub 32516 G=0.84555 A=0.15445
The PAGE Study Mexican Sub 10810 G=0.71119 A=0.28881
The PAGE Study Asian Sub 8318 G=0.9876 A=0.0124
The PAGE Study PuertoRican Sub 7918 G=0.7648 A=0.2352
The PAGE Study NativeHawaiian Sub 4534 G=0.9391 A=0.0609
The PAGE Study Cuban Sub 4228 G=0.7618 A=0.2382
The PAGE Study Dominican Sub 3828 G=0.7756 A=0.2244
The PAGE Study CentralAmerican Sub 2450 G=0.7118 A=0.2882
The PAGE Study SouthAmerican Sub 1982 G=0.7457 A=0.2543
The PAGE Study NativeAmerican Sub 1260 G=0.7794 A=0.2206
The PAGE Study SouthAsian Sub 856 G=0.800 A=0.200
14KJPN JAPANESE Study-wide 28258 G=0.99437 A=0.00563
8.3KJPN JAPANESE Study-wide 16760 G=0.99445 A=0.00555
1000Genomes_30x Global Study-wide 6404 G=0.8374 A=0.1626
1000Genomes_30x African Sub 1786 G=0.8483 A=0.1517
1000Genomes_30x Europe Sub 1266 G=0.7883 A=0.2117
1000Genomes_30x South Asian Sub 1202 G=0.8178 A=0.1822
1000Genomes_30x East Asian Sub 1170 G=0.9863 A=0.0137
1000Genomes_30x American Sub 980 G=0.728 A=0.272
1000Genomes Global Study-wide 5008 G=0.8397 A=0.1603
1000Genomes African Sub 1322 G=0.8495 A=0.1505
1000Genomes East Asian Sub 1008 G=0.9841 A=0.0159
1000Genomes Europe Sub 1006 G=0.7803 A=0.2197
1000Genomes South Asian Sub 978 G=0.819 A=0.181
1000Genomes American Sub 694 G=0.726 A=0.274
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.8364 A=0.1636
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.7883 A=0.2117
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.7740 A=0.2260
KOREAN population from KRGDB KOREAN Study-wide 2922 G=0.9880 A=0.0120
PharmGKB Aggregated Global Study-wide 2872 G=0.8155 A=0.1845
PharmGKB Aggregated PA155926095 Sub 2392 G=0.8115 A=0.1885
PharmGKB Aggregated PA152172450 Sub 480 G=0.835 A=0.165
HapMap Global Study-wide 1890 G=0.8661 A=0.1339
HapMap American Sub 768 G=0.849 A=0.151
HapMap African Sub 692 G=0.857 A=0.143
HapMap Asian Sub 254 G=0.984 A=0.016
HapMap Europe Sub 176 G=0.807 A=0.193
Korean Genome Project KOREAN Study-wide 1832 G=0.9880 A=0.0120
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.804 A=0.196
Northern Sweden ACPOP Study-wide 600 G=0.815 A=0.185
Qatari Global Study-wide 216 G=0.870 A=0.130
A Vietnamese Genetic Variation Database Global Study-wide 212 G=0.976 A=0.024
SGDP_PRJ Global Study-wide 136 G=0.449 A=0.551
The Danish reference pan genome Danish Study-wide 40 G=0.72 A=0.28
Siberian Global Study-wide 18 G=0.44 A=0.56
Help

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements
Sequence name Change
GRCh38.p14 chr 15 NC_000015.10:g.51324283G>A
GRCh37.p13 chr 15 NC_000015.9:g.51616480G>A
CYP19A1 RefSeqGene NG_007982.1:g.19316C>T
Gene: CYP19A1, cytochrome P450 family 19 subfamily A member 1 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
CYP19A1 transcript variant 1 NM_000103.4:c.-39+14212C>T N/A Intron Variant
CYP19A1 transcript variant 2 NM_031226.3:c.-147-359C>T N/A Intron Variant
CYP19A1 transcript variant 3 NM_001347248.1:c. N/A Genic Upstream Transcript Variant
CYP19A1 transcript variant 4 NM_001347249.2:c. N/A Genic Upstream Transcript Variant
CYP19A1 transcript variant 5 NM_001347250.2:c. N/A Genic Upstream Transcript Variant
CYP19A1 transcript variant 6 NM_001347251.2:c. N/A Genic Upstream Transcript Variant
CYP19A1 transcript variant 7 NM_001347252.2:c. N/A Genic Upstream Transcript Variant
CYP19A1 transcript variant 8 NM_001347253.2:c. N/A Genic Upstream Transcript Variant
CYP19A1 transcript variant 9 NM_001347254.2:c. N/A Genic Upstream Transcript Variant
CYP19A1 transcript variant 10 NM_001347255.2:c. N/A Genic Upstream Transcript Variant
CYP19A1 transcript variant 11 NM_001347256.2:c. N/A Genic Upstream Transcript Variant
Help

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar
Help

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement G= A
GRCh38.p14 chr 15 NC_000015.10:g.51324283= NC_000015.10:g.51324283G>A
GRCh37.p13 chr 15 NC_000015.9:g.51616480= NC_000015.9:g.51616480G>A
CYP19A1 RefSeqGene NG_007982.1:g.19316= NG_007982.1:g.19316C>T
CYP19A1 transcript variant 1 NM_000103.3:c.-39+14212= NM_000103.3:c.-39+14212C>T
CYP19A1 transcript variant 1 NM_000103.4:c.-39+14212= NM_000103.4:c.-39+14212C>T
CYP19A1 transcript variant 2 NM_031226.2:c.-147-359= NM_031226.2:c.-147-359C>T
CYP19A1 transcript variant 2 NM_031226.3:c.-147-359= NM_031226.3:c.-147-359C>T
Help

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

105 SubSNP, 22 Frequency submissions
No Submitter Submission ID Date (Build)
1 WI_SSAHASNP ss6587127 Feb 20, 2003 (111)
2 BCM_SSAHASNP ss10788081 Jul 11, 2003 (116)
3 EGP_SNPS ss35522012 May 24, 2005 (125)
4 ILLUMINA ss75156813 Dec 06, 2007 (129)
5 PHARMGKB_PPII ss84137968 Dec 15, 2007 (130)
6 PHARMGKB_PPII ss105109874 Feb 05, 2009 (130)
7 1000GENOMES ss108808116 Jan 23, 2009 (130)
8 ILLUMINA-UK ss118223229 Feb 14, 2009 (130)
9 KRIBB_YJKIM ss119487821 Dec 01, 2009 (131)
10 ILLUMINA ss160709969 Dec 01, 2009 (131)
11 COMPLETE_GENOMICS ss167989665 Jul 04, 2010 (132)
12 COMPLETE_GENOMICS ss171083837 Jul 04, 2010 (132)
13 ILLUMINA ss173807530 Jul 04, 2010 (132)
14 BUSHMAN ss200834519 Jul 04, 2010 (132)
15 1000GENOMES ss226889117 Jul 14, 2010 (132)
16 1000GENOMES ss236775659 Jul 15, 2010 (132)
17 1000GENOMES ss243162628 Jul 15, 2010 (132)
18 BL ss254976524 May 09, 2011 (134)
19 GMI ss286951675 Apr 25, 2013 (138)
20 ILLUMINA ss410935984 Sep 17, 2011 (135)
21 ILLUMINA ss481042128 May 04, 2012 (137)
22 ILLUMINA ss481063505 May 04, 2012 (137)
23 ILLUMINA ss482054067 Sep 08, 2015 (146)
24 ILLUMINA ss485316011 May 04, 2012 (137)
25 ILLUMINA ss537272191 Sep 08, 2015 (146)
26 SSMP ss660199812 Apr 25, 2013 (138)
27 ILLUMINA ss778546604 Sep 08, 2015 (146)
28 ILLUMINA ss783103837 Sep 08, 2015 (146)
29 ILLUMINA ss784061028 Sep 08, 2015 (146)
30 ILLUMINA ss832362441 Sep 08, 2015 (146)
31 ILLUMINA ss834003283 Sep 08, 2015 (146)
32 EVA-GONL ss991780260 Aug 21, 2014 (142)
33 JMKIDD_LAB ss1080120167 Aug 21, 2014 (142)
34 1000GENOMES ss1353442265 Aug 21, 2014 (142)
35 EVA_GENOME_DK ss1577611062 Apr 01, 2015 (144)
36 EVA_UK10K_ALSPAC ss1632984892 Apr 01, 2015 (144)
37 EVA_UK10K_TWINSUK ss1675978925 Apr 01, 2015 (144)
38 EVA_DECODE ss1695797580 Apr 01, 2015 (144)
39 EVA_SVP ss1713489350 Apr 01, 2015 (144)
40 ILLUMINA ss1752162871 Sep 08, 2015 (146)
41 WEILL_CORNELL_DGM ss1935183441 Feb 12, 2016 (147)
42 ILLUMINA ss1959612441 Feb 12, 2016 (147)
43 GENOMED ss1968104874 Jul 19, 2016 (147)
44 JJLAB ss2028371349 Sep 14, 2016 (149)
45 ILLUMINA ss2095058990 Dec 20, 2016 (150)
46 USC_VALOUEV ss2156773269 Dec 20, 2016 (150)
47 HUMAN_LONGEVITY ss2206732404 Dec 20, 2016 (150)
48 ILLUMINA ss2633227892 Nov 08, 2017 (151)
49 GNOMAD ss2934848549 Nov 08, 2017 (151)
50 AFFY ss2985041510 Nov 08, 2017 (151)
51 AFFY ss2985673036 Nov 08, 2017 (151)
52 SWEGEN ss3013273971 Nov 08, 2017 (151)
53 ILLUMINA ss3021632649 Nov 08, 2017 (151)
54 BIOINF_KMB_FNS_UNIBA ss3028009034 Nov 08, 2017 (151)
55 CSHL ss3351112521 Nov 08, 2017 (151)
56 ILLUMINA ss3627359501 Oct 12, 2018 (152)
57 ILLUMINA ss3631220973 Oct 12, 2018 (152)
58 ILLUMINA ss3633097094 Oct 12, 2018 (152)
59 ILLUMINA ss3633801693 Oct 12, 2018 (152)
60 ILLUMINA ss3634606439 Oct 12, 2018 (152)
61 ILLUMINA ss3635490608 Oct 12, 2018 (152)
62 ILLUMINA ss3636296306 Oct 12, 2018 (152)
63 ILLUMINA ss3637241883 Oct 12, 2018 (152)
64 ILLUMINA ss3638085354 Oct 12, 2018 (152)
65 ILLUMINA ss3640313760 Oct 12, 2018 (152)
66 ILLUMINA ss3643069614 Oct 12, 2018 (152)
67 ILLUMINA ss3652033284 Oct 12, 2018 (152)
68 ILLUMINA ss3652033285 Oct 12, 2018 (152)
69 ILLUMINA ss3653813178 Oct 12, 2018 (152)
70 EGCUT_WGS ss3680415418 Jul 13, 2019 (153)
71 EVA_DECODE ss3697881429 Jul 13, 2019 (153)
72 ILLUMINA ss3725499269 Jul 13, 2019 (153)
73 ACPOP ss3740918105 Jul 13, 2019 (153)
74 ILLUMINA ss3744906972 Jul 13, 2019 (153)
75 EVA ss3753077622 Jul 13, 2019 (153)
76 PAGE_CC ss3771829765 Jul 13, 2019 (153)
77 ILLUMINA ss3772405624 Jul 13, 2019 (153)
78 KHV_HUMAN_GENOMES ss3818395418 Jul 13, 2019 (153)
79 EVA ss3834231330 Apr 27, 2020 (154)
80 EVA ss3840714130 Apr 27, 2020 (154)
81 EVA ss3846202693 Apr 27, 2020 (154)
82 SGDP_PRJ ss3882905595 Apr 27, 2020 (154)
83 KRGDB ss3932070758 Apr 27, 2020 (154)
84 KOGIC ss3976132048 Apr 27, 2020 (154)
85 EVA ss4017701547 Apr 26, 2021 (155)
86 TOPMED ss4991212471 Apr 26, 2021 (155)
87 TOMMO_GENOMICS ss5216172304 Apr 26, 2021 (155)
88 EVA ss5237550676 Apr 26, 2021 (155)
89 1000G_HIGH_COVERAGE ss5298423509 Oct 16, 2022 (156)
90 EVA ss5315783250 Oct 16, 2022 (156)
91 EVA ss5419202840 Oct 16, 2022 (156)
92 HUGCELL_USP ss5492153386 Oct 16, 2022 (156)
93 EVA ss5511427969 Oct 16, 2022 (156)
94 1000G_HIGH_COVERAGE ss5599819429 Oct 16, 2022 (156)
95 SANFORD_IMAGENETICS ss5624360224 Oct 16, 2022 (156)
96 SANFORD_IMAGENETICS ss5657499035 Oct 16, 2022 (156)
97 TOMMO_GENOMICS ss5769972700 Oct 16, 2022 (156)
98 EVA ss5799937565 Oct 16, 2022 (156)
99 YY_MCH ss5815328206 Oct 16, 2022 (156)
100 EVA ss5828193925 Oct 16, 2022 (156)
101 EVA ss5847448518 Oct 16, 2022 (156)
102 EVA ss5847743048 Oct 16, 2022 (156)
103 EVA ss5875854948 Oct 16, 2022 (156)
104 EVA ss5948899197 Oct 16, 2022 (156)
105 EVA ss5979461022 Oct 16, 2022 (156)
106 1000Genomes NC_000015.9 - 51616480 Oct 12, 2018 (152)
107 1000Genomes_30x NC_000015.10 - 51324283 Oct 16, 2022 (156)
108 The Avon Longitudinal Study of Parents and Children NC_000015.9 - 51616480 Oct 12, 2018 (152)
109 Genetic variation in the Estonian population NC_000015.9 - 51616480 Oct 12, 2018 (152)
110 The Danish reference pan genome NC_000015.9 - 51616480 Apr 27, 2020 (154)
111 gnomAD - Genomes NC_000015.10 - 51324283 Apr 26, 2021 (155)
112 Genome of the Netherlands Release 5 NC_000015.9 - 51616480 Apr 27, 2020 (154)
113 HapMap NC_000015.10 - 51324283 Apr 27, 2020 (154)
114 KOREAN population from KRGDB NC_000015.9 - 51616480 Apr 27, 2020 (154)
115 Korean Genome Project NC_000015.10 - 51324283 Apr 27, 2020 (154)
116 Northern Sweden NC_000015.9 - 51616480 Jul 13, 2019 (153)
117 The PAGE Study NC_000015.10 - 51324283 Jul 13, 2019 (153)
118 PharmGKB Aggregated NC_000015.10 - 51324283 Apr 27, 2020 (154)
119 Qatari NC_000015.9 - 51616480 Apr 27, 2020 (154)
120 SGDP_PRJ NC_000015.9 - 51616480 Apr 27, 2020 (154)
121 Siberian NC_000015.9 - 51616480 Apr 27, 2020 (154)
122 8.3KJPN NC_000015.9 - 51616480 Apr 26, 2021 (155)
123 14KJPN NC_000015.10 - 51324283 Oct 16, 2022 (156)
124 TopMed NC_000015.10 - 51324283 Apr 26, 2021 (155)
125 UK 10K study - Twins NC_000015.9 - 51616480 Oct 12, 2018 (152)
126 A Vietnamese Genetic Variation Database NC_000015.9 - 51616480 Jul 13, 2019 (153)
127 ALFA NC_000015.10 - 51324283 Apr 26, 2021 (155)
Help

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID History Updated (Build)
rs58750380 May 24, 2008 (130)
rs386595317 Aug 21, 2014 (142)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss108808116, ss118223229, ss167989665, ss171083837, ss200834519, ss254976524, ss286951675, ss481042128, ss1695797580, ss1713489350, ss3643069614 NC_000015.8:49403771:G:A NC_000015.10:51324282:G:A (self)
66513693, 36922373, 26153666, 3853747, 16488800, 39248152, 14202970, 17225371, 34922575, 9289623, 74141611, 36922373, 8213920, ss226889117, ss236775659, ss243162628, ss481063505, ss482054067, ss485316011, ss537272191, ss660199812, ss778546604, ss783103837, ss784061028, ss832362441, ss834003283, ss991780260, ss1080120167, ss1353442265, ss1577611062, ss1632984892, ss1675978925, ss1752162871, ss1935183441, ss1959612441, ss1968104874, ss2028371349, ss2095058990, ss2156773269, ss2633227892, ss2934848549, ss2985041510, ss2985673036, ss3013273971, ss3021632649, ss3351112521, ss3627359501, ss3631220973, ss3633097094, ss3633801693, ss3634606439, ss3635490608, ss3636296306, ss3637241883, ss3638085354, ss3640313760, ss3652033284, ss3652033285, ss3653813178, ss3680415418, ss3740918105, ss3744906972, ss3753077622, ss3772405624, ss3834231330, ss3840714130, ss3882905595, ss3932070758, ss4017701547, ss5216172304, ss5237550676, ss5315783250, ss5419202840, ss5511427969, ss5624360224, ss5657499035, ss5799937565, ss5828193925, ss5847448518, ss5847743048, ss5948899197, ss5979461022 NC_000015.9:51616479:G:A NC_000015.10:51324282:G:A (self)
87345364, 468929130, 1262095, 32510049, 1051234, 3547, 103809804, 206758131, 7014447553, ss2206732404, ss3028009034, ss3697881429, ss3725499269, ss3771829765, ss3818395418, ss3846202693, ss3976132048, ss4991212471, ss5298423509, ss5492153386, ss5599819429, ss5769972700, ss5815328206, ss5875854948 NC_000015.10:51324282:G:A NC_000015.10:51324282:G:A (self)
ss10788081 NT_010194.15:22406090:G:A NC_000015.10:51324282:G:A (self)
ss6587127, ss35522012, ss75156813, ss84137968, ss105109874, ss119487821, ss160709969, ss173807530, ss410935984 NT_010194.17:22407036:G:A NC_000015.10:51324282:G:A (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

3 citations for rs4774585
PMID Title Author Year Journal
21170323 Aromatase gene polymorphisms are associated with survival among patients with cardiovascular disease in a sex-specific manner. Beitelshees AL et al. 2010 PloS one
23424626 Genetic variation and reproductive timing: African American women from the Population Architecture using Genomics and Epidemiology (PAGE) Study. Spencer KL et al. 2013 PloS one
26067721 Influence of CYP19A1 polymorphisms on the treatment of breast cancer with aromatase inhibitors: a systematic review and meta-analysis. Artigalás O et al. 2015 BMC medicine
Help

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:
Select flank length:

Genomic regions, transcripts, and products
Top▲ Help

NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Software version is: 2.0.1.post774+babeb33