rs199473183

Orientation

minus

Stabilized

minus

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

Make rs199473183(C;C)

Make rs199473183(C;T)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38581149

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473183
dbSNP (classic)	rs199473183
ClinGen	rs199473183
ebi	rs199473183
HLI	rs199473183
Exac	rs199473183
Gnomad	rs199473183
Varsome	rs199473183
LitVar	rs199473183
Map	rs199473183
PheGenI	rs199473183
Biobank	rs199473183
1000 genomes	rs199473183
hgdp	rs199473183
ensembl	rs199473183
geneview	rs199473183
scholar	rs199473183
google	rs199473183
pharmgkb	rs199473183
gwascentral	rs199473183
openSNP	rs199473183
23andMe	rs199473183
SNPshot	rs199473183
SNPdbe	rs199473183
MSV3d	rs199473183
GWAS Ctlg	rs199473183

Max Magnitude

0

ClinVar
Risk	rs199473183(C;C)
Alt	rs199473183(C;C)
Reference	Rs199473183(T;T)
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.38622640A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058543.3, RCV000155885.1,