rs199473569

Orientation

minus

Stabilized

minus

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

Make rs199473569(A;A)

Make rs199473569(A;C)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38606051

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473569
dbSNP (classic)	rs199473569
ClinGen	rs199473569
ebi	rs199473569
HLI	rs199473569
Exac	rs199473569
Gnomad	rs199473569
Varsome	rs199473569
LitVar	rs199473569
Map	rs199473569
PheGenI	rs199473569
Biobank	rs199473569
1000 genomes	rs199473569
hgdp	rs199473569
ensembl	rs199473569
geneview	rs199473569
scholar	rs199473569
google	rs199473569
pharmgkb	rs199473569
gwascentral	rs199473569
openSNP	rs199473569
23andMe	rs199473569
SNPshot	rs199473569
SNPdbe	rs199473569
MSV3d	rs199473569
GWAS Ctlg	rs199473569

Max Magnitude

0

ClinVar
Risk	rs199473569(A;A)
Alt	rs199473569(A;A)
Reference	Rs199473569(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.38647542G>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058410.3,