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Select item 11202651.

rs1120265 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:68671126 (GRCh38)
4:69536844 (GRCh37)
Canonical SPDI:: NC_000004.12:68671125:C:T
Gene:: UGT2B15 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.47722/7792 (ALFA)
C=0.15909/28 (SGDP_PRJ)
T=0.18072/30 (Qatari)
T=0.43079/1220 (KOREAN)
T=0.44429/2225 (1000Genomes)
C=0.45809/7677 (TOMMO)
HGVS:: NC_000004.12:g.68671126C>T, NC_000004.11:g.69536844C>T, NG_052676.1:g.4651G>A, NT_167250.2:g.247481T>C, NT_167250.1:g.249431T>C

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