rs370694515

Orientation

plus

Stabilized

plus

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

Make rs370694515(C;T)

Make rs370694515(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

38550679

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs370694515
dbSNP (classic)	rs370694515
ClinGen	rs370694515
ebi	rs370694515
HLI	rs370694515
Exac	rs370694515
Gnomad	rs370694515
Varsome	rs370694515
LitVar	rs370694515
Map	rs370694515
PheGenI	rs370694515
Biobank	rs370694515
1000 genomes	rs370694515
hgdp	rs370694515
ensembl	rs370694515
geneview	rs370694515
scholar	rs370694515
google	rs370694515
pharmgkb	rs370694515
gwascentral	rs370694515
openSNP	rs370694515
23andMe	rs370694515
SNPshot	rs370694515
SNPdbe	rs370694515
MSV3d	rs370694515
GWAS Ctlg	rs370694515

Max Magnitude

0

ClinVar
Risk	rs370694515(T;T)
Alt	rs370694515(T;T)
Reference	Rs370694515(C;C)
Significance	Pathogenic
Disease	not specified Long QT syndrome 3 Cardiovascular phenotype Arrhythmogenic right ventricular dysplasia/cardiomyopathy
Variation	info
Gene	SCN5A
CLNDBN	not specified Long QT syndrome 3 Cardiovascular phenotype Arrhythmogenic right ventricular dysplasia/cardiomyopathy
Reversed	0
HGVS	NC_000003.11:g.38592170C>T
CLNSRC
CLNACC	RCV000216249.1, RCV000234809.1, RCV000247589.1, RCV000466757.1,