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Select item 116804501.

rs11680450 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 2:233688837 (GRCh38)
2:234597483 (GRCh37)
Canonical SPDI:: NC_000002.12:233688836:T:A,NC_000002.12:233688836:T:C
Gene:: UGT1A10 (Varview), UGT1A8 (Varview), UGT1A7 (Varview), UGT1A9 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.399203/100140 (ALFA)
C=0.222222/48 (Vietnamese)
C=0.225944/742 (PRJEB37766)
C=0.228328/669 (KOREAN)
C=0.256406/4297 (TOMMO)
C=0.265228/209 (PRJEB37584)
C=0.341963/26905 (PAGE_STUDY)
C=0.361337/1810 (1000Genomes)
C=0.376493/99654 (TOPMED)
C=0.383192/725 (HapMap)
T=0.391447/119 (SGDP_PRJ)
C=0.392765/54936 (GnomAD)
C=0.398438/1785 (Estonian)
C=0.398867/1479 (TWINSUK)
C=0.406667/244 (NorthernSweden)
C=0.41483/414 (GoNL)
C=0.41645/1605 (ALSPAC)
T=0.416667/15 (Siberian)
C=0.416667/90 (Qatari)
C=0.45/18 (GENOME_DK)
HGVS:: NC_000002.12:g.233688837T>A, NC_000002.12:g.233688837T>C, NC_000002.11:g.234597483T>A, NC_000002.11:g.234597483T>C, NG_002601.2:g.104094T>A, NG_002601.2:g.104094T>C

dbSNP