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Select item 9890751.

rs989075 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,T [Show Flanks]
Chromosome:: 4:68667503 (GRCh38)
4:69533221 (GRCh37)
Canonical SPDI:: NC_000004.12:68667502:A:C,NC_000004.12:68667502:A:T
Gene:: UGT2B15 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.490659/9087 (ALFA)
A=0.327411/129 (SGDP_PRJ)
A=0.398148/86 (Qatari)
A=0.434319/7279 (TOMMO)
A=0.455497/2281 (1000Genomes)
T=0.460922/460 (GoNL)
A=0.472383/125035 (TOPMED)
A=0.47608/66237 (GnomAD)
T=0.499659/1464 (KOREAN)
A=0.5/3 (Siberian)
HGVS:: NC_000004.12:g.68667503A>C, NC_000004.12:g.68667503A>T, NC_000004.11:g.69533221A>C, NC_000004.11:g.69533221A>T, NG_052676.1:g.8274T>G, NG_052676.1:g.8274T>A, NT_167250.2:g.243859T>A, NT_167250.2:g.243859T>C, NT_167250.1:g.245809T>A, NT_167250.1:g.245809T>C

dbSNP