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Select item 124667471.

rs12466747 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 2:233698141 (GRCh38)
2:234606787 (GRCh37)
Canonical SPDI:: NC_000002.12:233698140:G:C
Gene:: UGT1A10 (Varview), UGT1A8 (Varview), UGT1A7 (Varview), UGT1A6 (Varview), UGT1A9 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.208999/3948 (ALFA)
C=0.11771/1973 (TOMMO)
C=0.125/27 (Qatari)
C=0.146758/430 (KOREAN)
C=0.147926/271 (Korea1K)
C=0.158537/52 (HapMap)
C=0.168801/845 (1000Genomes)
C=0.168922/44712 (TOPMED)
C=0.175655/24611 (GnomAD)
C=0.207415/207 (GoNL)
C=0.228964/849 (TWINSUK)
C=0.237416/915 (ALSPAC)
C=0.25/10 (GENOME_DK)
C=0.277778/60 (Vietnamese)
C=0.280134/1255 (Estonian)
C=0.303333/182 (NorthernSweden)
G=0.416667/10 (Siberian)
G=0.425/85 (SGDP_PRJ)
HGVS:: NC_000002.12:g.233698141G>C, NC_000002.11:g.234606787G>C, NG_002601.2:g.113398G>C

dbSNP