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Select item 75635611.

rs7563561 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 2:233690345 (GRCh38)
2:234598991 (GRCh37)
Canonical SPDI:: NC_000002.12:233690344:T:C,NC_000002.12:233690344:T:G
Gene:: UGT1A10 (Varview), UGT1A8 (Varview), UGT1A7 (Varview), UGT1A6 (Varview), UGT1A9 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.384983/56651 (ALFA)
G=0.228571/48 (Vietnamese)
G=0.22901/671 (KOREAN)
G=0.256477/4299 (TOMMO)
G=0.314696/197 (Chileans)
G=0.322097/172 (MGP)
G=0.326087/45 (PharmGKB)
G=0.361493/1810 (1000Genomes)
G=0.376777/99729 (TOPMED)
G=0.386581/726 (HapMap)
T=0.388158/118 (SGDP_PRJ)
G=0.393078/55016 (GnomAD)
G=0.397768/1782 (Estonian)
G=0.399137/1480 (TWINSUK)
G=0.406667/244 (NorthernSweden)
G=0.41483/414 (GoNL)
T=0.416667/15 (Siberian)
G=0.416667/90 (Qatari)
G=0.41671/1606 (ALSPAC)
G=0.45/18 (GENOME_DK)
HGVS:: NC_000002.12:g.233690345T>C, NC_000002.12:g.233690345T>G, NC_000002.11:g.234598991T>C, NC_000002.11:g.234598991T>G, NG_002601.2:g.105602T>C, NG_002601.2:g.105602T>G

dbSNP