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rs121907896

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121907896(A;A)
Make rs121907896(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position64591825
GeneSLC22A12
is asnp
is mentioned by
dbSNPrs121907896
ebirs121907896
HLIrs121907896
Exacrs121907896
Varsomers121907896
Maprs121907896
PheGenIrs121907896
hapmaprs121907896
1000 genomesrs121907896
hgdprs121907896
ensemblrs121907896
gopubmedrs121907896
geneviewrs121907896
scholarrs121907896
googlers121907896
pharmgkbrs121907896
gwascentralrs121907896
openSNPrs121907896
23andMers121907896
23andMe allrs121907896
SNP Nexus

SNPshotrs121907896
SNPdbers121907896
MSV3drs121907896
GWAS Ctlgrs121907896
Max Magnitude0
OMIM607096
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121907896(A;A)
Alt rs121907896(A;A)
Reference rs121907896(G;G)
Significance Pathogenic
Disease Familial renal hypouricemia
Variation info
Gene SLC22A12
CLNDBN Familial renal hypouricemia
Reversed 0
HGVS NC_000011.9:g.64359297G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003693.3,