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Select item 75881381.

rs7588138 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 2:233678328 (GRCh38)
2:234586974 (GRCh37)
Canonical SPDI:: NC_000002.12:233678327:A:T
Gene:: UGT1A10 (Varview), UGT1A8 (Varview), UGT1A9 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.373002/6908 (ALFA)
A=0.290323/126 (SGDP_PRJ)
A=0.3/12 (GENOME_DK)
A=0.303333/182 (NorthernSweden)
A=0.334152/1497 (Estonian)
T=0.373379/1094 (KOREAN)
T=0.374044/6269 (TOMMO)
A=0.378758/378 (GoNL)
A=0.388507/54084 (GnomAD)
A=0.404938/107183 (TOPMED)
A=0.424422/2126 (1000Genomes)
A=0.425926/92 (Qatari)
A=0.444444/8 (Siberian)
HGVS:: NC_000002.12:g.233678328A>T, NC_000002.11:g.234586974A>T, NG_002601.2:g.93585A>T

dbSNP