rs768579561

Merged into

rs483353016

Orientation

plus

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

Make rs768579561(C;T)

Make rs768579561(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

38562414

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs768579561
dbSNP (classic)	rs768579561
ClinGen	rs768579561
ebi	rs768579561
HLI	rs768579561
Exac	rs768579561
Gnomad	rs768579561
Varsome	rs768579561
LitVar	rs768579561
Map	rs768579561
PheGenI	rs768579561
Biobank	rs768579561
1000 genomes	rs768579561
hgdp	rs768579561
ensembl	rs768579561
geneview	rs768579561
scholar	rs768579561
google	rs768579561
pharmgkb	rs768579561
gwascentral	rs768579561
openSNP	rs768579561
23andMe	rs768579561
SNPshot	rs768579561
SNPdbe	rs768579561
MSV3d	rs768579561
GWAS Ctlg	rs768579561

Status

Merged into rs483353016

Max Magnitude

0

ClinVar
Risk	rs768579561(T;T)
Alt	rs768579561(T;T)
Reference	Rs768579561(C;C)
Significance	Probable-Pathogenic
Disease	not provided Brugada syndrome 1
Variation	info
Gene	SCN5A
CLNDBN	not provided Brugada syndrome 1
Reversed	0
HGVS	NC_000003.11:g.38603905C>T
CLNSRC
CLNACC	RCV000149447.1, RCV000155938.1,