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rs7932775

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs7932775(C;C)
Make rs7932775(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position64600390
GeneSLC22A12
is asnp
is mentioned by
dbSNPrs7932775
dbSNP (old)rs7932775
ClinGenrs7932775
ebirs7932775
HLIrs7932775
Exacrs7932775
Gnomadrs7932775
Varsomers7932775
Maprs7932775
PheGenIrs7932775
Biobankrs7932775
1000 genomesrs7932775
hgdprs7932775
ensemblrs7932775
gopubmedrs7932775
geneviewrs7932775
scholarrs7932775
googlers7932775
pharmgkbrs7932775
gwascentralrs7932775
openSNPrs7932775
23andMers7932775
23andMe allrs7932775
SNP Nexus

SNPshotrs7932775
SNPdbers7932775
MSV3drs7932775
GWAS Ctlgrs7932775
GMAF0.376
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 19833602] Multiple single nucleotide polymorphisms in the human urate transporter 1 (hURAT1) gene are associated with hyperuricemia in Han Chinese

[PMID 21154327] [Association of the exon 8 and intron 8 polymorphisms of the human urate transporter 1 gene with primary hyperuricemia in Chinese Han population].


ClinVar
Risk rs7932775(C;C) rs7932775(G;G)
Alt rs7932775(C;C) rs7932775(G;G)
Reference Rs7932775(T;T)
Significance Non-pathogenic
Disease Familial renal hypouricemia
Variation info
Gene SLC22A12
CLNDBN Familial renal hypouricemia
Reversed 0
HGVS NC_000011.9:g.64367862T>C
CLNSRC
CLNACC RCV000300784.1,