rs137853342

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs137853342(A;A)

Make rs137853342(A;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

23215237

Gene

SCNN1G

is a	snp
is	mentioned by
dbSNP	rs137853342
dbSNP (classic)	rs137853342
ClinGen	rs137853342
ebi	rs137853342
HLI	rs137853342
Exac	rs137853342
Gnomad	rs137853342
Varsome	rs137853342
LitVar	rs137853342
Map	rs137853342
PheGenI	rs137853342
Biobank	rs137853342
1000 genomes	rs137853342
hgdp	rs137853342
ensembl	rs137853342
geneview	rs137853342
scholar	rs137853342
google	rs137853342
pharmgkb	rs137853342
gwascentral	rs137853342
openSNP	rs137853342
23andMe	rs137853342
SNPshot	rs137853342
SNPdbe	rs137853342
MSV3d	rs137853342
GWAS Ctlg	rs137853342

Max Magnitude

0

OMIM	600761
Desc
Variant	0001
Related	also

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,