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Select item 455206381.

rs45520638 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 2:233636231 (GRCh38)
2:234544877 (GRCh37)
Canonical SPDI:: NC_000002.12:233636230:G:A,NC_000002.12:233636230:G:T
Gene:: UGT1A10 (Varview), UGT1A8 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000092/3 (ALFA)
A=0.00037/98 (TOPMED)
A=0.007463/1 (PharmGKB)
HGVS:: NC_000002.12:g.233636231G>A, NC_000002.12:g.233636231G>T, NC_000002.11:g.234544877G>A, NC_000002.11:g.234544877G>T, NG_002601.2:g.51488G>A, NG_002601.2:g.51488G>T

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