rs794728891

Orientation

minus

Stabilized

minus

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

Make rs794728891(C;C)

Make rs794728891(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

38551300

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs794728891
dbSNP (classic)	rs794728891
ClinGen	rs794728891
ebi	rs794728891
HLI	rs794728891
Exac	rs794728891
Gnomad	rs794728891
Varsome	rs794728891
LitVar	rs794728891
Map	rs794728891
PheGenI	rs794728891
Biobank	rs794728891
1000 genomes	rs794728891
hgdp	rs794728891
ensembl	rs794728891
geneview	rs794728891
scholar	rs794728891
google	rs794728891
pharmgkb	rs794728891
gwascentral	rs794728891
openSNP	rs794728891
23andMe	rs794728891
SNPshot	rs794728891
SNPdbe	rs794728891
MSV3d	rs794728891
GWAS Ctlg	rs794728891

Max Magnitude

0

ClinVar
Risk	rs794728891(C;C)
Alt	rs794728891(C;C)
Reference	Rs794728891(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN5A
CLNDBN	not provided
Reversed	1
HGVS	NC_000003.11:g.38592791A>G
CLNSRC
CLNACC	RCV000183099.2,