Have questions? Visit https://www.reddit.com/r/SNPedia

rs121907893

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121907893(C;T)
Make rs121907893(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position64593548
GeneSLC22A12
is asnp
is mentioned by
dbSNPrs121907893
ebirs121907893
HLIrs121907893
Exacrs121907893
Varsomers121907893
Maprs121907893
PheGenIrs121907893
hapmaprs121907893
1000 genomesrs121907893
hgdprs121907893
ensemblrs121907893
gopubmedrs121907893
geneviewrs121907893
scholarrs121907893
googlers121907893
pharmgkbrs121907893
gwascentralrs121907893
openSNPrs121907893
23andMers121907893
23andMe allrs121907893
SNP Nexus

SNPshotrs121907893
SNPdbers121907893
MSV3drs121907893
GWAS Ctlgrs121907893
Max Magnitude0
OMIM607096
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121907893(T;T)
Alt rs121907893(T;T)
Reference rs121907893(C;C)
Significance Pathogenic
Disease Familial renal hypouricemia
Variation info
Gene SLC22A12
CLNDBN Familial renal hypouricemia
Reversed 0
HGVS NC_000011.9:g.64361020C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003690.3,