rs794728867

Orientation

minus

Stabilized

minus

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

Make rs794728867(C;C)

Make rs794728867(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

38585762

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs794728867
dbSNP (classic)	rs794728867
ClinGen	rs794728867
ebi	rs794728867
HLI	rs794728867
Exac	rs794728867
Gnomad	rs794728867
Varsome	rs794728867
LitVar	rs794728867
Map	rs794728867
PheGenI	rs794728867
Biobank	rs794728867
1000 genomes	rs794728867
hgdp	rs794728867
ensembl	rs794728867
geneview	rs794728867
scholar	rs794728867
google	rs794728867
pharmgkb	rs794728867
gwascentral	rs794728867
openSNP	rs794728867
23andMe	rs794728867
SNPshot	rs794728867
SNPdbe	rs794728867
MSV3d	rs794728867
GWAS Ctlg	rs794728867

Max Magnitude

0

ClinVar
Risk	rs794728867(C;C)
Alt	rs794728867(C;C)
Reference	Rs794728867(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN5A
CLNDBN	not provided
Reversed	1
HGVS	NC_000003.11:g.38627253A>G
CLNSRC
CLNACC	RCV000183010.1,