rs45589741

Orientation

minus

Stabilized

minus

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

Make rs45589741(C;C)

Make rs45589741(C;T)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38566501

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs45589741
dbSNP (classic)	rs45589741
ClinGen	rs45589741
ebi	rs45589741
HLI	rs45589741
Exac	rs45589741
Gnomad	rs45589741
Varsome	rs45589741
LitVar	rs45589741
Map	rs45589741
PheGenI	rs45589741
Biobank	rs45589741
1000 genomes	rs45589741
hgdp	rs45589741
ensembl	rs45589741
geneview	rs45589741
scholar	rs45589741
google	rs45589741
pharmgkb	rs45589741
gwascentral	rs45589741
openSNP	rs45589741
23andMe	rs45589741
SNPshot	rs45589741
SNPdbe	rs45589741
MSV3d	rs45589741
GWAS Ctlg	rs45589741

Max Magnitude

0

ClinVar
Risk	rs45589741(C;C)
Alt	rs45589741(C;C)
Reference	Rs45589741(T;T)
Significance	Untested
Disease	Acquired long QT syndrome
Variation	info
Gene	SCN5A
CLNDBN	Acquired long QT syndrome
Reversed	1
HGVS	NC_000003.11:g.38607992A>G
CLNSRC	ClinVar
CLNACC	RCV000058598.3,