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rs137852707

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852707(C;C)
Make rs137852707(C;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position23380736
GeneSCNN1B
is asnp
is mentioned by
dbSNPrs137852707
ebirs137852707
HLIrs137852707
Exacrs137852707
Varsomers137852707
Maprs137852707
PheGenIrs137852707
hapmaprs137852707
1000 genomesrs137852707
hgdprs137852707
ensemblrs137852707
gopubmedrs137852707
geneviewrs137852707
scholarrs137852707
googlers137852707
pharmgkbrs137852707
gwascentralrs137852707
openSNPrs137852707
23andMers137852707
23andMe allrs137852707
SNP Nexus

SNPshotrs137852707
SNPdbers137852707
MSV3drs137852707
GWAS Ctlgrs137852707
Max Magnitude0
OMIM600760
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137852707(C;C)
Alt rs137852707(C;C)
Reference rs137852707(T;T)
Significance Pathogenic
Disease Pseudoprimary hyperaldosteronism
Variation info
Gene SCNN1B
CLNDBN Pseudoprimary hyperaldosteronism
Reversed 0
HGVS NC_000016.9:g.23392057T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000009381.3,