rs199473099

Orientation

minus

Stabilized

minus

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

Make rs199473099(C;T)

Make rs199473099(T;T)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38606700

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473099
dbSNP (classic)	rs199473099
ClinGen	rs199473099
ebi	rs199473099
HLI	rs199473099
Exac	rs199473099
Gnomad	rs199473099
Varsome	rs199473099
LitVar	rs199473099
Map	rs199473099
PheGenI	rs199473099
Biobank	rs199473099
1000 genomes	rs199473099
hgdp	rs199473099
ensembl	rs199473099
geneview	rs199473099
scholar	rs199473099
google	rs199473099
pharmgkb	rs199473099
gwascentral	rs199473099
openSNP	rs199473099
23andMe	rs199473099
SNPshot	rs199473099
SNPdbe	rs199473099
MSV3d	rs199473099
GWAS Ctlg	rs199473099

Max Magnitude

0

ClinVar
Risk	rs199473099(T;T)
Alt	rs199473099(T;T)
Reference	Rs199473099(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.38648191G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058393.3,