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Select item 16041441.

rs1604144 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:233697189 (GRCh38)
2:234605835 (GRCh37)
Canonical SPDI:: NC_000002.12:233697188:C:T
Gene:: UGT1A10 (Varview), UGT1A8 (Varview), UGT1A7 (Varview), UGT1A6 (Varview), UGT1A9 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.296185/35214 (ALFA)
T=0.139555/2339 (TOMMO)
T=0.19215/563 (KOREAN)
T=0.199236/365 (Korea1K)
T=0.25/6 (PRJEB36033)
T=0.279271/582 (HGDP_Stanford)
T=0.284569/284 (GoNL)
T=0.291667/63 (Qatari)
T=0.302589/1122 (TWINSUK)
T=0.312143/1203 (ALSPAC)
T=0.330009/87350 (TOPMED)
T=0.331215/46325 (GnomAD)
T=0.332265/622 (HapMap)
T=0.333854/1672 (1000Genomes)
T=0.336161/1506 (Estonian)
T=0.353774/75 (Vietnamese)
T=0.363333/218 (NorthernSweden)
C=0.397959/117 (SGDP_PRJ)
C=0.423077/11 (Siberian)
T=0.425/17 (GENOME_DK)
HGVS:: NC_000002.12:g.233697189C>T, NC_000002.11:g.234605835C>T, NG_002601.2:g.112446C>T

dbSNP