rs7932775

plus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs7932775(C;C)

Make rs7932775(C;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

64600390

Gene

SLC22A12

is a	snp
is	mentioned by
dbSNP	rs7932775
dbSNP (classic)	rs7932775
ClinGen	rs7932775
ebi	rs7932775
HLI	rs7932775
Exac	rs7932775
Gnomad	rs7932775
Varsome	rs7932775
LitVar	rs7932775
Map	rs7932775
PheGenI	rs7932775
Biobank	rs7932775
1000 genomes	rs7932775
hgdp	rs7932775
ensembl	rs7932775
geneview	rs7932775
scholar	rs7932775
google	rs7932775
pharmgkb	rs7932775
gwascentral	rs7932775
openSNP	rs7932775
23andMe	rs7932775
SNPshot	rs7932775
SNPdbe	rs7932775
MSV3d	rs7932775
GWAS Ctlg	rs7932775

GMAF

0.376

Max Magnitude

0

?

(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,