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rs121907895

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121907895(G;G)
Make rs121907895(G;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position64599858
GeneSLC22A12
is asnp
is mentioned by
dbSNPrs121907895
ebirs121907895
HLIrs121907895
Exacrs121907895
Varsomers121907895
Maprs121907895
PheGenIrs121907895
hapmaprs121907895
1000 genomesrs121907895
hgdprs121907895
ensemblrs121907895
gopubmedrs121907895
geneviewrs121907895
scholarrs121907895
googlers121907895
pharmgkbrs121907895
gwascentralrs121907895
openSNPrs121907895
23andMers121907895
23andMe allrs121907895
SNP Nexus

SNPshotrs121907895
SNPdbers121907895
MSV3drs121907895
GWAS Ctlgrs121907895
Max Magnitude0
OMIM607096
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121907895(C,G;C,G)
Alt rs121907895(C,G;C,G)
Reference rs121907895(T;T)
Significance Pathogenic
Disease Familial renal hypouricemia
Variation info
Gene SLC22A12
CLNDBN Familial renal hypouricemia
Reversed 0
HGVS NC_000011.9:g.64367330T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000003692.3,