rs137852704

Orientation

plus

Stabilized

plus

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

Make rs137852704(C;T)

Make rs137852704(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

23380574

Gene

SCNN1B

is a	snp
is	mentioned by
dbSNP	rs137852704
dbSNP (classic)	rs137852704
ClinGen	rs137852704
ebi	rs137852704
HLI	rs137852704
Exac	rs137852704
Gnomad	rs137852704
Varsome	rs137852704
LitVar	rs137852704
Map	rs137852704
PheGenI	rs137852704
Biobank	rs137852704
1000 genomes	rs137852704
hgdp	rs137852704
ensembl	rs137852704
geneview	rs137852704
scholar	rs137852704
google	rs137852704
pharmgkb	rs137852704
gwascentral	rs137852704
openSNP	rs137852704
23andMe	rs137852704
SNPshot	rs137852704
SNPdbe	rs137852704
MSV3d	rs137852704
GWAS Ctlg	rs137852704

Max Magnitude

0

OMIM	600760
Desc
Variant	0001
Related	also

ClinVar
Risk	rs137852704(G;G) rs137852704(T;T)
Alt	rs137852704(G;G) rs137852704(T;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	RCV000009378.4,