rs199473109

Orientation

minus

Stabilized

minus

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

Make rs199473109(C;G)

Make rs199473109(G;G)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38606064

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473109
dbSNP (classic)	rs199473109
ClinGen	rs199473109
ebi	rs199473109
HLI	rs199473109
Exac	rs199473109
Gnomad	rs199473109
Varsome	rs199473109
LitVar	rs199473109
Map	rs199473109
PheGenI	rs199473109
Biobank	rs199473109
1000 genomes	rs199473109
hgdp	rs199473109
ensembl	rs199473109
geneview	rs199473109
scholar	rs199473109
google	rs199473109
pharmgkb	rs199473109
gwascentral	rs199473109
openSNP	rs199473109
23andMe	rs199473109
SNPshot	rs199473109
SNPdbe	rs199473109
MSV3d	rs199473109
GWAS Ctlg	rs199473109

Max Magnitude

0

ClinVar
Risk	rs199473109(G;G)
Alt	rs199473109(G;G)
Reference	Rs199473109(C;C)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	SCN5A
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000003.11:g.38647555G>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058407.3,