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rs559946

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs559946(A;G)
Make rs559946(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position64591133
GeneSLC22A12
is asnp
is mentioned by
dbSNPrs559946
dbSNP (old)rs559946
ClinGenrs559946
ebirs559946
HLIrs559946
Exacrs559946
Gnomadrs559946
Varsomers559946
Maprs559946
PheGenIrs559946
Biobankrs559946
1000 genomesrs559946
hgdprs559946
ensemblrs559946
gopubmedrs559946
geneviewrs559946
scholarrs559946
googlers559946
pharmgkbrs559946
gwascentralrs559946
openSNPrs559946
23andMers559946
23andMe allrs559946
SNP Nexus

SNPshotrs559946
SNPdbers559946
MSV3drs559946
GWAS Ctlgrs559946
GMAF0.4545
Max Magnitude0

[PMID 23981340] The hURAT1 rs559946 polymorphism and the incidence of gout in Han Chinese men

ClinVar
Risk rs559946(G;G)
Alt rs559946(G;G)
Reference Rs559946(A;A)
Significance Non-pathogenic
Disease Familial renal hypouricemia
Variation info
Gene SLC22A12
CLNDBN Familial renal hypouricemia
Reversed 1
HGVS NC_000011.9:g.64358605T>C
CLNSRC
CLNACC RCV000339005.1,