rs6599230

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common (and likely to be benign)
(T;T)	0	common in clinvar

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

38633221

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs6599230
dbSNP (classic)	rs6599230
ClinGen	rs6599230
ebi	rs6599230
HLI	rs6599230
Exac	rs6599230
Gnomad	rs6599230
Varsome	rs6599230
LitVar	rs6599230
Map	rs6599230
PheGenI	rs6599230
Biobank	rs6599230
1000 genomes	rs6599230
hgdp	rs6599230
ensembl	rs6599230
geneview	rs6599230
scholar	rs6599230
google	rs6599230
pharmgkb	rs6599230
gwascentral	rs6599230
openSNP	rs6599230
23andMe	rs6599230
SNPshot	rs6599230
SNPdbe	rs6599230
MSV3d	rs6599230
GWAS Ctlg	rs6599230

Max Magnitude

0

[PMID 26401487] Mutational analysis of SCN5A gene in long QT syndrome

[PMID 26497660] Novel association of polymorphic genetic variants with predictors of outcome of catheter ablation in atrial fibrillation: new directions from a prospective study (DECAF)

ClinVar
Risk	Rs6599230(C;C)
Alt	Rs6599230(C;C)
Reference	Rs6599230(T;T)
Significance	Probable-non-pathogenic
Disease	not specified Cardiovascular phenotype Romano-Ward syndrome Sick sinus syndrome Brugada syndrome Progressive familial heart block Paroxysmal familial ventricular fibrillation Dilated Cardiomyopathy Long QT syndrome
Variation	info
Gene	SCN5A
CLNDBN	not specified Cardiovascular phenotype Romano-Ward syndrome Sick sinus syndrome Brugada syndrome Progressive familial heart block Paroxysmal familial ventricular fibrillation Dilated Cardiomyopathy, Dominant Long QT syndrome
Reversed	0
HGVS	NC_000003.11:g.38674712T>C
CLNSRC
CLNACC	RCV000041640.9, RCV000249089.1, RCV000289272.1, RCV000292966.1, RCV000344291.1, RCV000347707.1, RCV000383571.1, RCV000387171.1, RCV000408022.1,