rs199473641

Orientation

minus

Stabilized

minus

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

Make rs199473641(A;G)

Make rs199473641(G;G)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38581061

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473641
ClinGen	rs199473641
ebi	rs199473641
HLI	rs199473641
Exac	rs199473641
Varsome	rs199473641
Map	rs199473641
PheGenI	rs199473641
hapmap	rs199473641
1000 genomes	rs199473641
hgdp	rs199473641
ensembl	rs199473641
gopubmed	rs199473641
geneview	rs199473641
scholar	rs199473641
google	rs199473641
pharmgkb	rs199473641
gwascentral	rs199473641
openSNP	rs199473641
23andMe	rs199473641
23andMe all	rs199473641
SNP Nexus
SNPshot	rs199473641
SNPdbe	rs199473641
MSV3d	rs199473641
GWAS Ctlg	rs199473641

Max Magnitude

0

ClinVar
Risk	rs199473641(G;G)
Alt	rs199473641(G;G)
Reference	Rs199473641(A;A)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	SCN5A
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000003.11:g.38622552T>C
CLNSRC	ClinVar
CLNACC	RCV000058547.3,