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rs121917740

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917740(C;T)
Make rs121917740(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position204155078
GeneREN
is asnp
is mentioned by
dbSNPrs121917740
ebirs121917740
HLIrs121917740
Exacrs121917740
Varsomers121917740
Maprs121917740
PheGenIrs121917740
hapmaprs121917740
1000 genomesrs121917740
hgdprs121917740
ensemblrs121917740
gopubmedrs121917740
geneviewrs121917740
scholarrs121917740
googlers121917740
pharmgkbrs121917740
gwascentralrs121917740
openSNPrs121917740
23andMers121917740
23andMe allrs121917740
SNP Nexus

SNPshotrs121917740
SNPdbers121917740
MSV3drs121917740
GWAS Ctlgrs121917740
Max Magnitude0
OMIM179820
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121917740(T;T)
Alt rs121917740(T;T)
Reference rs121917740(C;C)
Significance Pathogenic
Disease Hyperproreninemia
Variation info
Gene REN
CLNDBN Hyperproreninemia, familial
Reversed 1
HGVS NC_000001.10:g.204124206G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014002.24,