rs137852708

Orientation

plus

Stabilized

plus

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

Make rs137852708(C;T)

Make rs137852708(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

23380727

Gene

SCNN1B

is a	snp
is	mentioned by
dbSNP	rs137852708
dbSNP (classic)	rs137852708
ClinGen	rs137852708
ebi	rs137852708
HLI	rs137852708
Exac	rs137852708
Gnomad	rs137852708
Varsome	rs137852708
LitVar	rs137852708
Map	rs137852708
PheGenI	rs137852708
Biobank	rs137852708
1000 genomes	rs137852708
hgdp	rs137852708
ensembl	rs137852708
geneview	rs137852708
scholar	rs137852708
google	rs137852708
pharmgkb	rs137852708
gwascentral	rs137852708
openSNP	rs137852708
23andMe	rs137852708
SNPshot	rs137852708
SNPdbe	rs137852708
MSV3d	rs137852708
GWAS Ctlg	rs137852708

Max Magnitude

0

OMIM	600760
Desc
Variant	0007
Related	also

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 UniProtKB (protein)
CLNACC	RCV000009384.4,