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Select item 454645941.

rs45464594 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 2:233635922 (GRCh38)
2:234544568 (GRCh37)
Canonical SPDI:: NC_000002.12:233635921:G:T
Gene:: UGT1A10 (Varview), UGT1A8 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.012002/443 (ALFA)
T=0.013889/3 (Qatari)
T=0.017872/2484 (GnomAD)
T=0.019181/5077 (TOPMED)
T=0.027483/138 (1000Genomes)
T=0.052239/7 (PharmGKB)
G=0.5/3 (SGDP_PRJ)
HGVS:: NC_000002.12:g.233635922G>T, NC_000002.11:g.234544568G>T, NG_002601.2:g.51179G>T

dbSNP