rs199473277

Orientation

minus

Stabilized

minus

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

Make rs199473277(C;C)

Make rs199473277(C;T)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38554311

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473277
dbSNP (classic)	rs199473277
ClinGen	rs199473277
ebi	rs199473277
HLI	rs199473277
Exac	rs199473277
Gnomad	rs199473277
Varsome	rs199473277
LitVar	rs199473277
Map	rs199473277
PheGenI	rs199473277
Biobank	rs199473277
1000 genomes	rs199473277
hgdp	rs199473277
ensembl	rs199473277
geneview	rs199473277
scholar	rs199473277
google	rs199473277
pharmgkb	rs199473277
gwascentral	rs199473277
openSNP	rs199473277
23andMe	rs199473277
SNPshot	rs199473277
SNPdbe	rs199473277
MSV3d	rs199473277
GWAS Ctlg	rs199473277

Max Magnitude

0

ClinVar
Risk	rs199473277(C;C)
Alt	rs199473277(C;C)
Reference	Rs199473277(T;T)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	SCN5A
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000003.11:g.38595802A>G
CLNSRC	ClinVar
CLNACC	RCV000058704.3,