Name: rs17129472
Published: September 21, 2022
License: Open Access

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.

rs17129472

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:66816506 (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=0.123764 (32759/264690, TOPMED)
A=0.126291 (17659/139828, GnomAD)
A=0.14212 (11799/83024, ALFA) (+ 18 more)
A=0.19768 (5586/28258, 14KJPN)
A=0.19618 (3288/16760, 8.3KJPN)
A=0.1463 (937/6404, 1000G_30x)
A=0.1538 (770/5008, 1000G)
A=0.1520 (681/4480, Estonian)
A=0.1336 (515/3854, ALSPAC)
A=0.1508 (559/3708, TWINSUK)
A=0.1816 (532/2930, KOREAN)
A=0.2011 (419/2084, HGDP_Stanford)
A=0.1368 (258/1886, HapMap)
A=0.1752 (321/1832, Korea1K)
A=0.149 (149/998, GoNL)
A=0.157 (94/600, NorthernSweden)
A=0.111 (24/216, Qatari)
G=0.423 (83/196, SGDP_PRJ)
A=0.17 (7/40, GENOME_DK)
G=0.38 (10/26, Siberian)
A=0.0 (0/4, Ancient Sardinia)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DNAI4 : Intron Variant
Publications: 0 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: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	83024	G=0.85788	A=0.14212
European	Sub	69186	G=0.85822	A=0.14178
African	Sub	4724	G=0.9492	A=0.0508
African Others	Sub	180	G=0.967	A=0.033
African American	Sub	4544	G=0.9485	A=0.0515
Asian	Sub	202	G=0.782	A=0.218
East Asian	Sub	160	G=0.812	A=0.188
Other Asian	Sub	42	G=0.67	A=0.33
Latin American 1	Sub	268	G=0.854	A=0.146
Latin American 2	Sub	1316	G=0.7872	A=0.2128
South Asian	Sub	4958	G=0.7927	A=0.2073
Other	Sub	2370	G=0.8485	A=0.1515

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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	G=0.876236	A=0.123764
gnomAD - Genomes	Global	Study-wide	139828	G=0.873709	A=0.126291
gnomAD - Genomes	European	Sub	75716	G=0.84665	A=0.15335
gnomAD - Genomes	African	Sub	41898	G=0.95334	A=0.04666
gnomAD - Genomes	American	Sub	13620	G=0.80932	A=0.19068
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	G=0.8423	A=0.1577
gnomAD - Genomes	East Asian	Sub	3120	G=0.7849	A=0.2151
gnomAD - Genomes	Other	Sub	2152	G=0.8601	A=0.1399
Allele Frequency Aggregator	Total	Global	83024	G=0.85788	A=0.14212
Allele Frequency Aggregator	European	Sub	69186	G=0.85822	A=0.14178
Allele Frequency Aggregator	South Asian	Sub	4958	G=0.7927	A=0.2073
Allele Frequency Aggregator	African	Sub	4724	G=0.9492	A=0.0508
Allele Frequency Aggregator	Other	Sub	2370	G=0.8485	A=0.1515
Allele Frequency Aggregator	Latin American 2	Sub	1316	G=0.7872	A=0.2128
Allele Frequency Aggregator	Latin American 1	Sub	268	G=0.854	A=0.146
Allele Frequency Aggregator	Asian	Sub	202	G=0.782	A=0.218
14KJPN	JAPANESE	Study-wide	28258	G=0.80232	A=0.19768
8.3KJPN	JAPANESE	Study-wide	16760	G=0.80382	A=0.19618
1000Genomes_30x	Global	Study-wide	6404	G=0.8537	A=0.1463
1000Genomes_30x	African	Sub	1786	G=0.9742	A=0.0258
1000Genomes_30x	Europe	Sub	1266	G=0.8689	A=0.1311
1000Genomes_30x	South Asian	Sub	1202	G=0.7903	A=0.2097
1000Genomes_30x	East Asian	Sub	1170	G=0.7641	A=0.2359
1000Genomes_30x	American	Sub	980	G=0.799	A=0.201
1000Genomes	Global	Study-wide	5008	G=0.8462	A=0.1538
1000Genomes	African	Sub	1322	G=0.9720	A=0.0280
1000Genomes	East Asian	Sub	1008	G=0.7659	A=0.2341
1000Genomes	Europe	Sub	1006	G=0.8608	A=0.1392
1000Genomes	South Asian	Sub	978	G=0.781	A=0.219
1000Genomes	American	Sub	694	G=0.794	A=0.206
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.8480	A=0.1520
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.8664	A=0.1336
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.8492	A=0.1508
KOREAN population from KRGDB	KOREAN	Study-wide	2930	G=0.8184	A=0.1816
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	G=0.7989	A=0.2011
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	G=0.740	A=0.260
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	G=0.826	A=0.174
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	G=0.866	A=0.134
HGDP-CEPH-db Supplement 1	Europe	Sub	320	G=0.866	A=0.134
HGDP-CEPH-db Supplement 1	Africa	Sub	242	G=0.946	A=0.054
HGDP-CEPH-db Supplement 1	America	Sub	216	G=0.519	A=0.481
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	G=0.75	A=0.25
HapMap	Global	Study-wide	1886	G=0.8632	A=0.1368
HapMap	American	Sub	770	G=0.822	A=0.178
HapMap	African	Sub	690	G=0.949	A=0.051
HapMap	Asian	Sub	250	G=0.748	A=0.252
HapMap	Europe	Sub	176	G=0.869	A=0.131
Korean Genome Project	KOREAN	Study-wide	1832	G=0.8248	A=0.1752
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.851	A=0.149
Northern Sweden	ACPOP	Study-wide	600	G=0.843	A=0.157
Qatari	Global	Study-wide	216	G=0.889	A=0.111
SGDP_PRJ	Global	Study-wide	196	G=0.423	A=0.577
The Danish reference pan genome	Danish	Study-wide	40	G=0.82	A=0.17
Siberian	Global	Study-wide	26	G=0.38	A=0.62
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	4	G=1.0	A=0.0

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 1	NC_000001.11:g.66816506G>A
GRCh37.p13 chr 1	NC_000001.10:g.67282189G>A

Gene: DNAI4, dynein axonemal intermediate chain 4 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DNAI4 transcript variant 1	NM_024763.5:c.2497-2326C>T	N/A	Intron Variant
DNAI4 transcript variant 2	NM_207014.3:c.	N/A	Genic Downstream Transcript Variant
DNAI4 transcript variant X4	XM_005271212.4:c.2302-232… XM_005271212.4:c.2302-2326C>T	N/A	Intron Variant
DNAI4 transcript variant X1	XM_011542161.3:c.2410-232… XM_011542161.3:c.2410-2326C>T	N/A	Intron Variant
DNAI4 transcript variant X2	XM_011542162.3:c.2398-232… XM_011542162.3:c.2398-2326C>T	N/A	Intron Variant
DNAI4 transcript variant X7	XM_017002353.2:c.2203-232… XM_017002353.2:c.2203-2326C>T	N/A	Intron Variant
DNAI4 transcript variant X8	XM_017002354.2:c.2116-232… XM_017002354.2:c.2116-2326C>T	N/A	Intron Variant
DNAI4 transcript variant X9	XM_017002355.1:c.1735-232… XM_017002355.1:c.1735-2326C>T	N/A	Intron Variant
DNAI4 transcript variant X10	XM_024449821.2:c.1630-232… XM_024449821.2:c.1630-2326C>T	N/A	Intron Variant
DNAI4 transcript variant X3	XM_047430731.1:c.2311-232… XM_047430731.1:c.2311-2326C>T	N/A	Intron Variant
DNAI4 transcript variant X5	XM_047430749.1:c.2281-232… XM_047430749.1:c.2281-2326C>T	N/A	Intron Variant
DNAI4 transcript variant X6	XM_047430752.1:c.2215-232… XM_047430752.1:c.2215-2326C>T	N/A	Intron Variant
DNAI4 transcript variant X11	XM_017002357.2:c.	N/A	Genic Downstream Transcript Variant

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

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 1	NC_000001.11:g.66816506=	NC_000001.11:g.66816506G>A
GRCh37.p13 chr 1	NC_000001.10:g.67282189=	NC_000001.10:g.67282189G>A
WDR78 transcript variant 1	NM_024763.4:c.2497-2326=	NM_024763.4:c.2497-2326C>T
DNAI4 transcript variant 1	NM_024763.5:c.2497-2326=	NM_024763.5:c.2497-2326C>T
WDR78 transcript variant X1	XM_005271212.1:c.2302-2326=	XM_005271212.1:c.2302-2326C>T
DNAI4 transcript variant X4	XM_005271212.4:c.2302-2326=	XM_005271212.4:c.2302-2326C>T
WDR78 transcript variant X4	XM_005271213.1:c.1630-2326=	XM_005271213.1:c.1630-2326C>T
DNAI4 transcript variant X1	XM_011542161.3:c.2410-2326=	XM_011542161.3:c.2410-2326C>T
DNAI4 transcript variant X2	XM_011542162.3:c.2398-2326=	XM_011542162.3:c.2398-2326C>T
DNAI4 transcript variant X7	XM_017002353.2:c.2203-2326=	XM_017002353.2:c.2203-2326C>T
DNAI4 transcript variant X8	XM_017002354.2:c.2116-2326=	XM_017002354.2:c.2116-2326C>T
DNAI4 transcript variant X9	XM_017002355.1:c.1735-2326=	XM_017002355.1:c.1735-2326C>T
DNAI4 transcript variant X10	XM_024449821.2:c.1630-2326=	XM_024449821.2:c.1630-2326C>T
DNAI4 transcript variant X3	XM_047430731.1:c.2311-2326=	XM_047430731.1:c.2311-2326C>T
DNAI4 transcript variant X5	XM_047430749.1:c.2281-2326=	XM_047430749.1:c.2281-2326C>T
DNAI4 transcript variant X6	XM_047430752.1:c.2215-2326=	XM_047430752.1:c.2215-2326C>T

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#.

83 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PERLEGEN	ss23849777	Sep 20, 2004 (123)
2	ILLUMINA	ss67178209	Dec 01, 2006 (127)
3	ILLUMINA	ss67541089	Dec 01, 2006 (127)
4	ILLUMINA	ss68175221	Dec 12, 2006 (127)
5	PERLEGEN	ss68769171	May 17, 2007 (127)
6	ILLUMINA	ss70656233	May 25, 2008 (130)
7	ILLUMINA	ss71216124	May 17, 2007 (127)
8	AFFY	ss74854995	Aug 16, 2007 (128)
9	ILLUMINA	ss75530907	Dec 07, 2007 (129)
10	KRIBB_YJKIM	ss85367520	Dec 15, 2007 (130)
11	BGI	ss102749310	Feb 23, 2009 (131)
12	ILLUMINA	ss153634398	Dec 01, 2009 (131)
13	ILLUMINA	ss159309907	Dec 01, 2009 (131)
14	ILLUMINA	ss172758632	Jul 04, 2010 (132)
15	1000GENOMES	ss218430851	Jul 14, 2010 (132)
16	1000GENOMES	ss230568187	Jul 14, 2010 (132)
17	1000GENOMES	ss238256373	Jul 15, 2010 (132)
18	GMI	ss275859558	May 04, 2012 (137)
19	ILLUMINA	ss482386200	May 04, 2012 (137)
20	ILLUMINA	ss483977872	May 04, 2012 (137)
21	ILLUMINA	ss536171444	Sep 08, 2015 (146)
22	TISHKOFF	ss554206700	Apr 25, 2013 (138)
23	SSMP	ss648079714	Apr 25, 2013 (138)
24	ILLUMINA	ss780479996	Sep 08, 2015 (146)
25	ILLUMINA	ss782433101	Sep 08, 2015 (146)
26	ILLUMINA	ss832821969	Jul 12, 2019 (153)
27	ILLUMINA	ss835970499	Sep 08, 2015 (146)
28	EVA-GONL	ss975246657	Aug 21, 2014 (142)
29	JMKIDD_LAB	ss1067953599	Aug 21, 2014 (142)
30	1000GENOMES	ss1291220545	Aug 21, 2014 (142)
31	DDI	ss1425837340	Apr 01, 2015 (144)
32	EVA_GENOME_DK	ss1574120516	Apr 01, 2015 (144)
33	EVA_DECODE	ss1584616090	Apr 01, 2015 (144)
34	EVA_UK10K_ALSPAC	ss1600348955	Apr 01, 2015 (144)
35	EVA_UK10K_TWINSUK	ss1643342988	Apr 01, 2015 (144)
36	EVA_SVP	ss1712340228	Apr 01, 2015 (144)
37	HAMMER_LAB	ss1794495530	Sep 08, 2015 (146)
38	WEILL_CORNELL_DGM	ss1918454676	Feb 12, 2016 (147)
39	JJLAB	ss2019744684	Sep 14, 2016 (149)
40	USC_VALOUEV	ss2147760445	Dec 20, 2016 (150)
41	HUMAN_LONGEVITY	ss2163187932	Dec 20, 2016 (150)
42	ILLUMINA	ss2632526831	Nov 08, 2017 (151)
43	GRF	ss2697678075	Nov 08, 2017 (151)
44	GNOMAD	ss2756072839	Nov 08, 2017 (151)
45	SWEGEN	ss2986948320	Nov 08, 2017 (151)
46	BIOINF_KMB_FNS_UNIBA	ss3023634124	Nov 08, 2017 (151)
47	CSHL	ss3343492797	Nov 08, 2017 (151)
48	ILLUMINA	ss3626117301	Oct 11, 2018 (152)
49	ILLUMINA	ss3630562436	Oct 11, 2018 (152)
50	ILLUMINA	ss3637762047	Oct 11, 2018 (152)
51	ILLUMINA	ss3638899980	Oct 11, 2018 (152)
52	ILLUMINA	ss3639762288	Oct 11, 2018 (152)
53	ILLUMINA	ss3641594354	Oct 11, 2018 (152)
54	ILLUMINA	ss3642773703	Oct 11, 2018 (152)
55	ILLUMINA	ss3643815976	Oct 11, 2018 (152)
56	EGCUT_WGS	ss3655018294	Jul 12, 2019 (153)
57	EVA_DECODE	ss3686933321	Jul 12, 2019 (153)
58	ACPOP	ss3727119221	Jul 12, 2019 (153)
59	EVA	ss3746306296	Jul 12, 2019 (153)
60	PACBIO	ss3783432864	Jul 12, 2019 (153)
61	PACBIO	ss3789087514	Jul 12, 2019 (153)
62	PACBIO	ss3793960296	Jul 12, 2019 (153)
63	KHV_HUMAN_GENOMES	ss3799313003	Jul 12, 2019 (153)
64	EVA	ss3826214555	Apr 25, 2020 (154)
65	HGDP	ss3847336521	Apr 25, 2020 (154)
66	SGDP_PRJ	ss3849019031	Apr 25, 2020 (154)
67	KRGDB	ss3894046487	Apr 25, 2020 (154)
68	KOGIC	ss3944672870	Apr 25, 2020 (154)
69	EVA	ss3984802191	Apr 25, 2021 (155)
70	EVA	ss4016915313	Apr 25, 2021 (155)
71	TOPMED	ss4452627742	Apr 25, 2021 (155)
72	TOMMO_GENOMICS	ss5144317416	Apr 25, 2021 (155)
73	1000G_HIGH_COVERAGE	ss5242553724	Oct 12, 2022 (156)
74	EVA	ss5314622308	Oct 12, 2022 (156)
75	HUGCELL_USP	ss5443588406	Oct 12, 2022 (156)
76	1000G_HIGH_COVERAGE	ss5514973543	Oct 12, 2022 (156)
77	SANFORD_IMAGENETICS	ss5625692343	Oct 12, 2022 (156)
78	TOMMO_GENOMICS	ss5669194536	Oct 12, 2022 (156)
79	YY_MCH	ss5800668143	Oct 12, 2022 (156)
80	EVA	ss5832070259	Oct 12, 2022 (156)
81	EVA	ss5848941670	Oct 12, 2022 (156)
82	EVA	ss5908589473	Oct 12, 2022 (156)
83	EVA	ss5937530992	Oct 12, 2022 (156)
84	1000Genomes	NC_000001.10 - 67282189	Oct 11, 2018 (152)
85	1000Genomes_30x	NC_000001.11 - 66816506	Oct 12, 2022 (156)
86	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 67282189	Oct 11, 2018 (152)
87	Genetic variation in the Estonian population	NC_000001.10 - 67282189	Oct 11, 2018 (152)
88	The Danish reference pan genome	NC_000001.10 - 67282189	Apr 25, 2020 (154)
89	gnomAD - Genomes	NC_000001.11 - 66816506	Apr 25, 2021 (155)
90	Genome of the Netherlands Release 5	NC_000001.10 - 67282189	Apr 25, 2020 (154)
91	HGDP-CEPH-db Supplement 1	NC_000001.9 - 67054777	Apr 25, 2020 (154)
92	HapMap	NC_000001.11 - 66816506	Apr 25, 2020 (154)
93	KOREAN population from KRGDB	NC_000001.10 - 67282189	Apr 25, 2020 (154)
94	Korean Genome Project	NC_000001.11 - 66816506	Apr 25, 2020 (154)
95	Northern Sweden	NC_000001.10 - 67282189	Jul 12, 2019 (153)
96	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000001.10 - 67282189	Apr 25, 2021 (155)
97	Qatari	NC_000001.10 - 67282189	Apr 25, 2020 (154)
98	SGDP_PRJ	NC_000001.10 - 67282189	Apr 25, 2020 (154)
99	Siberian	NC_000001.10 - 67282189	Apr 25, 2020 (154)
100	8.3KJPN	NC_000001.10 - 67282189	Apr 25, 2021 (155)
101	14KJPN	NC_000001.11 - 66816506	Oct 12, 2022 (156)
102	TopMed	NC_000001.11 - 66816506	Apr 25, 2021 (155)
103	UK 10K study - Twins	NC_000001.10 - 67282189	Oct 11, 2018 (152)
104	ALFA	NC_000001.11 - 66816506	Apr 25, 2021 (155)

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)
rs52837993	Sep 21, 2007 (128)
rs58982329	May 25, 2008 (130)
rs74225041	Dec 02, 2009 (131)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3638899980, ss3639762288, ss3643815976	NC_000001.8:66994209:G:A	NC_000001.11:66816505:G:A	(self)
14413, ss275859558, ss482386200, ss1584616090, ss1712340228, ss3642773703, ss3847336521	NC_000001.9:67054776:G:A	NC_000001.11:66816505:G:A	(self)
1950578, 1068655, 756542, 1536109, 456164, 1223881, 404086, 28118, 496606, 1036011, 276799, 2286723, 1068655, ss218430851, ss230568187, ss238256373, ss483977872, ss536171444, ss554206700, ss648079714, ss780479996, ss782433101, ss832821969, ss835970499, ss975246657, ss1067953599, ss1291220545, ss1425837340, ss1574120516, ss1600348955, ss1643342988, ss1794495530, ss1918454676, ss2019744684, ss2147760445, ss2632526831, ss2697678075, ss2756072839, ss2986948320, ss3343492797, ss3626117301, ss3630562436, ss3637762047, ss3641594354, ss3655018294, ss3727119221, ss3746306296, ss3783432864, ss3789087514, ss3793960296, ss3826214555, ss3849019031, ss3894046487, ss3984802191, ss4016915313, ss5144317416, ss5314622308, ss5625692343, ss5832070259, ss5937530992	NC_000001.10:67282188:G:A	NC_000001.11:66816505:G:A	(self)
2499478, 13754361, 87820, 1050871, 3031640, 16234077, 13618208737, ss2163187932, ss3023634124, ss3686933321, ss3799313003, ss3944672870, ss4452627742, ss5242553724, ss5443588406, ss5514973543, ss5669194536, ss5800668143, ss5848941670, ss5908589473	NC_000001.11:66816505:G:A	NC_000001.11:66816505:G:A	(self)
ss23849777, ss67178209, ss67541089, ss68175221, ss68769171, ss70656233, ss71216124, ss74854995, ss75530907, ss85367520, ss102749310, ss153634398, ss159309907, ss172758632	NT_032977.9:37254106:G:A	NC_000001.11:66816505:G:A	(self)

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

No publications for rs17129472

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
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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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs17129472