rs137852705

Orientation

plus

Stabilized

plus

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

Make rs137852705(C;T)

Make rs137852705(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

23380731

Gene

SCNN1B

is a	snp
is	mentioned by
dbSNP	rs137852705
dbSNP (classic)	rs137852705
ClinGen	rs137852705
ebi	rs137852705
HLI	rs137852705
Exac	rs137852705
Gnomad	rs137852705
Varsome	rs137852705
LitVar	rs137852705
Map	rs137852705
PheGenI	rs137852705
Biobank	rs137852705
1000 genomes	rs137852705
hgdp	rs137852705
ensembl	rs137852705
geneview	rs137852705
scholar	rs137852705
google	rs137852705
pharmgkb	rs137852705
gwascentral	rs137852705
openSNP	rs137852705
23andMe	rs137852705
SNPshot	rs137852705
SNPdbe	rs137852705
MSV3d	rs137852705
GWAS Ctlg	rs137852705

Max Magnitude

0

OMIM	600760
Desc
Variant	0002
Related	also

OMIM	600760
Desc
Variant	0008
Related	also

ClinVar
Risk	rs137852705(G;G) rs137852705(T;T)
Alt	rs137852705(G;G) rs137852705(T;T)
Reference	Rs137852705(C;C)
Significance	Untested
Disease
Variation	info
Gene	SCNN1B
CLNDBN
Reversed	0
HGVS	NC_000016.9:g.23392052C>G; NC_000016.9:g.23392052C>T
CLNSRC
CLNACC