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Select item 10548051.

rs1054805 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 2:233743017 (GRCh38)
2:234651663 (GRCh37)
Canonical SPDI:: NC_000002.12:233743016:T:C,NC_000002.12:233743016:T:G
Gene:: UGT1A10 (Varview), UGT1A8 (Varview), UGT1A7 (Varview), UGT1A6 (Varview), UGT1A5 (Varview), UGT1A9 (Varview), UGT1A4 (Varview), UGT1A3 (Varview), DNAJB3 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0./0 (HapMap)
G=0.000008/2 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000002.12:g.233743017T>C, NC_000002.12:g.233743017T>G, NC_000002.11:g.234651663T>C, NC_000002.11:g.234651663T>G, NG_002601.2:g.158274T>C, NG_002601.2:g.158274T>G, NM_001001394.4:c.*462A>G, NM_001001394.4:c.*462A>C, NM_001001394.3:c.*462A>G, NM_001001394.3:c.*462A>C, NR_172931.1:n.982A>G, NR_172931.1:n.982A>C

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