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rs137852704

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852704(C;T)
Make rs137852704(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position23380574
GeneSCNN1B
is asnp
is mentioned by
dbSNPrs137852704
ebirs137852704
HLIrs137852704
Exacrs137852704
Varsomers137852704
Maprs137852704
PheGenIrs137852704
hapmaprs137852704
1000 genomesrs137852704
hgdprs137852704
ensemblrs137852704
gopubmedrs137852704
geneviewrs137852704
scholarrs137852704
googlers137852704
pharmgkbrs137852704
gwascentralrs137852704
openSNPrs137852704
23andMers137852704
23andMe allrs137852704
SNP Nexus

SNPshotrs137852704
SNPdbers137852704
MSV3drs137852704
GWAS Ctlgrs137852704
Max Magnitude0
OMIM600760
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137852704(G,T;G,T)
Alt rs137852704(G,T;G,T)
Reference rs137852704(C;C)
Significance Pathogenic
Disease Pseudoprimary hyperaldosteronism
Variation info
Gene SCNN1B
CLNDBN Pseudoprimary hyperaldosteronism
Reversed 0
HGVS NC_000016.9:g.23391895C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009378.3,