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Select item 178647051.

rs17864705 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 2:233763682 (GRCh38)
2:234672328 (GRCh37)
Canonical SPDI:: NC_000002.12:233763681:G:T
Gene:: UGT1A10 (Varview), UGT1A8 (Varview), UGT1A7 (Varview), UGT1A6 (Varview), UGT1A5 (Varview), UGT1A9 (Varview), UGT1A4 (Varview), UGT1A1 (Varview), UGT1A3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.064479/3494 (ALFA)
T=0.042084/42 (GoNL)
T=0.05/30 (NorthernSweden)
T=0.053668/199 (TWINSUK)
T=0.055804/250 (Estonian)
T=0.057343/221 (ALSPAC)
T=0.062446/8751 (GnomAD)
T=0.069512/18399 (TOPMED)
T=0.1/4 (GENOME_DK)
T=0.100423/190 (HapMap)
T=0.114772/575 (1000Genomes)
T=0.125/27 (Qatari)
T=0.129141/2164 (TOMMO)
T=0.149147/437 (KOREAN)
T=0.158843/291 (Korea1K)
T=0.261682/56 (Vietnamese)
G=0.448718/70 (SGDP_PRJ)
G=0.5/3 (Siberian)
HGVS:: NC_000002.12:g.233763682G>T, NC_000002.11:g.234672328G>T, NG_002601.2:g.178939G>T, NG_033238.1:g.8410G>T

dbSNP