rs199473630

Orientation

minus

Stabilized

minus

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

Make rs199473630(A;A)

Make rs199473630(A;G)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38551133

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473630
dbSNP (classic)	rs199473630
ClinGen	rs199473630
ebi	rs199473630
HLI	rs199473630
Exac	rs199473630
Gnomad	rs199473630
Varsome	rs199473630
LitVar	rs199473630
Map	rs199473630
PheGenI	rs199473630
Biobank	rs199473630
1000 genomes	rs199473630
hgdp	rs199473630
ensembl	rs199473630
geneview	rs199473630
scholar	rs199473630
google	rs199473630
pharmgkb	rs199473630
gwascentral	rs199473630
openSNP	rs199473630
23andMe	rs199473630
SNPshot	rs199473630
SNPdbe	rs199473630
MSV3d	rs199473630
GWAS Ctlg	rs199473630

Max Magnitude

0

ClinVar
Risk	rs199473630(A;A)
Alt	rs199473630(A;A)
Reference	Rs199473630(G;G)
Significance	Untested
Disease	Congenital long QT syndrome not specified
Variation	info
Gene	SCN5A
CLNDBN	Congenital long QT syndrome not specified
Reversed	1
HGVS	NC_000003.11:g.38592624C>T
CLNSRC	ClinVar
CLNACC	RCV000058756.3, RCV000183111.2,