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rs137853342

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853342(A;A)
Make rs137853342(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position23215237
GeneSCNN1G
is asnp
is mentioned by
dbSNPrs137853342
ebirs137853342
HLIrs137853342
Exacrs137853342
Varsomers137853342
Maprs137853342
PheGenIrs137853342
hapmaprs137853342
1000 genomesrs137853342
hgdprs137853342
ensemblrs137853342
gopubmedrs137853342
geneviewrs137853342
scholarrs137853342
googlers137853342
pharmgkbrs137853342
gwascentralrs137853342
openSNPrs137853342
23andMers137853342
23andMe allrs137853342
SNP Nexus

SNPshotrs137853342
SNPdbers137853342
MSV3drs137853342
GWAS Ctlgrs137853342
Max Magnitude0
OMIM600761
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137853342(A;A)
Alt rs137853342(A;A)
Reference rs137853342(G;G)
Significance Pathogenic
Disease Pseudoprimary hyperaldosteronism
Variation info
Gene SCNN1G
CLNDBN Pseudoprimary hyperaldosteronism
Reversed 0
HGVS NC_000016.9:g.23226558G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009372.3,