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Select item 359152711.

rs35915271 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 2:233764965 (GRCh38)
2:234673611 (GRCh37)
Canonical SPDI:: NC_000002.12:233764964:A:G,NC_000002.12:233764964:A: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=0.001352/19 (ALFA)
T=0.001541/408 (TOPMED)
T=0.001564/217 (GnomAD)
T=0.001718/11 (1000Genomes)
HGVS:: NC_000002.12:g.233764965A>G, NC_000002.12:g.233764965A>T, NC_000002.11:g.234673611A>G, NC_000002.11:g.234673611A>T, NG_002601.2:g.180222A>G, NG_002601.2:g.180222A>T, NG_033238.1:g.9693A>G, NG_033238.1:g.9693A>T

dbSNP