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Select item 134319131.

rs13431913 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 2:233649566 (GRCh38)
2:234558212 (GRCh37)
Canonical SPDI:: NC_000002.12:233649565:G:A,NC_000002.12:233649565:G:T
Gene:: UGT1A10 (Varview), UGT1A8 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.007282/1058 (ALFA)
A=0.027778/6 (Qatari)
A=0.028004/3925 (GnomAD)
A=0.029162/7719 (TOPMED)
A=0.031855/160 (1000Genomes)
A=0.066824/85 (HapMap)
G=0.416667/5 (SGDP_PRJ)
HGVS:: NC_000002.12:g.233649566G>A, NC_000002.12:g.233649566G>T, NC_000002.11:g.234558212G>A, NC_000002.11:g.234558212G>T, NG_002601.2:g.64823G>A, NG_002601.2:g.64823G>T

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