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rs7932775

From SNPedia

Orientationplus
Stabilizedplus
Make rs7932775(C;C)
Make rs7932775(C;T)
Make rs7932775(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position64600390
GeneSLC22A12
is asnp
is mentioned by
dbSNPrs7932775
ebirs7932775
HLIrs7932775
Exacrs7932775
Varsomers7932775
Maprs7932775
PheGenIrs7932775
hapmaprs7932775
1000 genomesrs7932775
hgdprs7932775
ensemblrs7932775
gopubmedrs7932775
geneviewrs7932775
scholarrs7932775
googlers7932775
pharmgkbrs7932775
gwascentralrs7932775
openSNPrs7932775
23andMers7932775
23andMe allrs7932775
SNP Nexus

SNPshotrs7932775
SNPdbers7932775
MSV3drs7932775
GWAS Ctlgrs7932775
GMAF0.376
Max Magnitude
? (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].