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Select item 116751681.

rs11675168 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:233756033 (GRCh38)
2:234664679 (GRCh37)
Canonical SPDI:: NC_000002.12:233756032:G:A
Gene:: UGT1A10 (Varview), UGT1A8 (Varview), UGT1A7 (Varview), UGT1A6 (Varview), UGT1A5 (Varview), UGT1A9 (Varview), UGT1A4 (Varview), UGT1A3 (Varview), LOC100286922 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.028458/4125 (ALFA)
A=0.000342/1 (KOREAN)
A=0.006871/34 (1000Genomes)
A=0.012376/10 (HapMap)
A=0.013889/3 (Qatari)
A=0.018361/4860 (TOPMED)
A=0.020091/2817 (GnomAD)
A=0.029839/115 (ALSPAC)
A=0.030744/114 (TWINSUK)
A=0.031667/19 (NorthernSweden)
A=0.034068/34 (GoNL)
G=0.5/7 (SGDP_PRJ)
HGVS:: NC_000002.12:g.233756033G>A, NC_000002.11:g.234664679G>A, NG_002601.2:g.171290G>A, NG_033238.1:g.761G>A

dbSNP