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rs121907897

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121907897(G;T)
Make rs121907897(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position64599687
GeneSLC22A12
is asnp
is mentioned by
dbSNPrs121907897
ebirs121907897
HLIrs121907897
Exacrs121907897
Varsomers121907897
Maprs121907897
PheGenIrs121907897
hapmaprs121907897
1000 genomesrs121907897
hgdprs121907897
ensemblrs121907897
gopubmedrs121907897
geneviewrs121907897
scholarrs121907897
googlers121907897
pharmgkbrs121907897
gwascentralrs121907897
openSNPrs121907897
23andMers121907897
23andMe allrs121907897
SNP Nexus

SNPshotrs121907897
SNPdbers121907897
MSV3drs121907897
GWAS Ctlgrs121907897
Max Magnitude0
OMIM607096
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121907897(T;T)
Alt rs121907897(T;T)
Reference rs121907897(G;G)
Significance Pathogenic
Disease Familial renal hypouricemia
Variation info
Gene SLC22A12
CLNDBN Familial renal hypouricemia
Reversed 0
HGVS NC_000011.9:g.64367159G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003694.3,