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rs137852708

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852708(C;T)
Make rs137852708(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position23380727
GeneSCNN1B
is asnp
is mentioned by
dbSNPrs137852708
ebirs137852708
HLIrs137852708
Exacrs137852708
Varsomers137852708
Maprs137852708
PheGenIrs137852708
hapmaprs137852708
1000 genomesrs137852708
hgdprs137852708
ensemblrs137852708
gopubmedrs137852708
geneviewrs137852708
scholarrs137852708
googlers137852708
pharmgkbrs137852708
gwascentralrs137852708
openSNPrs137852708
23andMers137852708
23andMe allrs137852708
SNP Nexus

SNPshotrs137852708
SNPdbers137852708
MSV3drs137852708
GWAS Ctlgrs137852708
Max Magnitude0
OMIM600760
Desc
Variant0007
Relatedalso
ClinVar
Risk rs137852708(T;T)
Alt rs137852708(T;T)
Reference rs137852708(C;C)
Significance Pathogenic
Disease Pseudoprimary hyperaldosteronism
Variation info
Gene SCNN1B
CLNDBN Pseudoprimary hyperaldosteronism
Reversed 0
HGVS NC_000016.9:g.23392048C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009384.4,