rs878855296

Orientation

minus

Stabilized

minus

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

Make rs878855296(A;A)

Make rs878855296(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

38613790

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs878855296
dbSNP (classic)	rs878855296
ClinGen	rs878855296
ebi	rs878855296
HLI	rs878855296
Exac	rs878855296
Gnomad	rs878855296
Varsome	rs878855296
LitVar	rs878855296
Map	rs878855296
PheGenI	rs878855296
Biobank	rs878855296
1000 genomes	rs878855296
hgdp	rs878855296
ensembl	rs878855296
geneview	rs878855296
scholar	rs878855296
google	rs878855296
pharmgkb	rs878855296
gwascentral	rs878855296
openSNP	rs878855296
23andMe	rs878855296
SNPshot	rs878855296
SNPdbe	rs878855296
MSV3d	rs878855296
GWAS Ctlg	rs878855296

Max Magnitude

0

ClinVar
Risk	rs878855296(A;A)
Alt	rs878855296(A;A)
Reference	Rs878855296(G;G)
Significance	Pathogenic
Disease	Brugada syndrome not provided
Variation	info
Gene	SCN5A
CLNDBN	Brugada syndrome not provided
Reversed	1
HGVS	NC_000003.11:g.38655281C>T
CLNSRC
CLNACC	RCV000226209.2, RCV000494338.1,