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rs11231825

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs11231825(C;C)
Make rs11231825(C;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position64592802
GeneSLC22A12
is asnp
is mentioned by
dbSNPrs11231825
dbSNP (classic)rs11231825
ClinGenrs11231825
ebirs11231825
HLIrs11231825
Exacrs11231825
Gnomadrs11231825
Varsomers11231825
LitVarrs11231825
Maprs11231825
PheGenIrs11231825
Biobankrs11231825
1000 genomesrs11231825
hgdprs11231825
ensemblrs11231825
geneviewrs11231825
scholarrs11231825
googlers11231825
pharmgkbrs11231825
gwascentralrs11231825
openSNPrs11231825
23andMers11231825
SNPshotrs11231825
SNPdbers11231825
MSV3drs11231825
GWAS Ctlgrs11231825
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 25128519] Tubular urate transporter gene polymorphisms differentiate patients with gout who have normal and decreased urinary uric acid excretion


ClinVar
Risk rs11231825(C;C)
Alt rs11231825(C;C)
Reference Rs11231825(T;T)
Significance Non-pathogenic
Disease Familial renal hypouricemia
Variation info
Gene SLC22A12
CLNDBN Familial renal hypouricemia
Reversed 0
HGVS NC_000011.9:g.64360274T>C
CLNSRC
CLNACC RCV000286659.1,