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

rs121907892

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121907892(A;A)
Make rs121907892(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position64593747
GeneSLC22A12
is asnp
is mentioned by
dbSNPrs121907892
ebirs121907892
HLIrs121907892
Exacrs121907892
Varsomers121907892
Maprs121907892
PheGenIrs121907892
hapmaprs121907892
1000 genomesrs121907892
hgdprs121907892
ensemblrs121907892
gopubmedrs121907892
geneviewrs121907892
scholarrs121907892
googlers121907892
pharmgkbrs121907892
gwascentralrs121907892
openSNPrs121907892
23andMers121907892
23andMe allrs121907892
SNP Nexus

SNPshotrs121907892
SNPdbers121907892
MSV3drs121907892
GWAS Ctlgrs121907892
GMAF0.001837
Max Magnitude0
OMIM607096
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121907892(A;A)
Alt rs121907892(A;A)
Reference rs121907892(G;G)
Significance Pathogenic
Disease Familial renal hypouricemia
Variation info
Gene SLC22A12
CLNDBN Familial renal hypouricemia
Reversed 0
HGVS NC_000011.9:g.64361219G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003689.3,