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rs13113918

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs13113918(A;G)
Make rs13113918(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position9996869
GeneLOC105374476, SLC2A9
is asnp
is mentioned by
dbSNPrs13113918
dbSNP (classic)rs13113918
ClinGenrs13113918
ebirs13113918
HLIrs13113918
Exacrs13113918
Gnomadrs13113918
Varsomers13113918
LitVarrs13113918
Maprs13113918
PheGenIrs13113918
Biobankrs13113918
1000 genomesrs13113918
hgdprs13113918
ensemblrs13113918
geneviewrs13113918
scholarrs13113918
googlers13113918
pharmgkbrs13113918
gwascentralrs13113918
openSNPrs13113918
23andMers13113918
SNPshotrs13113918
SNPdbers13113918
MSV3drs13113918
GWAS Ctlgrs13113918
GMAF0.1607
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 21186168OA-icon.png] Association between SLC2A9 transporter gene variants and uric acid phenotypes in African American and white families


[PMID 23272134OA-icon.png] Changes in uric acid levels following bariatric surgery are not associated with SLC2A9 variants in the Swedish Obese Subjects Study


ClinVar
Risk rs13113918(G;G)
Alt rs13113918(G;G)
Reference Rs13113918(A;A)
Significance Non-pathogenic
Disease Familial renal hypouricemia
Variation info
Gene SLC2A9
CLNDBN Familial renal hypouricemia
Reversed 0
HGVS NC_000004.11:g.9998493A>G
CLNSRC
CLNACC RCV000320934.1,