rs199473551

Orientation

minus

Stabilized

minus

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

Make rs199473551(A;G)

Make rs199473551(G;G)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38633219

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473551
dbSNP (classic)	rs199473551
ClinGen	rs199473551
ebi	rs199473551
HLI	rs199473551
Exac	rs199473551
Gnomad	rs199473551
Varsome	rs199473551
LitVar	rs199473551
Map	rs199473551
PheGenI	rs199473551
Biobank	rs199473551
1000 genomes	rs199473551
hgdp	rs199473551
ensembl	rs199473551
geneview	rs199473551
scholar	rs199473551
google	rs199473551
pharmgkb	rs199473551
gwascentral	rs199473551
openSNP	rs199473551
23andMe	rs199473551
SNPshot	rs199473551
SNPdbe	rs199473551
MSV3d	rs199473551
GWAS Ctlg	rs199473551

Max Magnitude

0

ClinVar
Risk	rs199473551(G;G)
Alt	rs199473551(G;G)
Reference	Rs199473551(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.38674710T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058861.3,