rs199473308

Orientation

minus

Stabilized

minus

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

Make rs199473308(A;A)

Make rs199473308(A;T)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38551090

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473308
dbSNP (classic)	rs199473308
ClinGen	rs199473308
ebi	rs199473308
HLI	rs199473308
Exac	rs199473308
Gnomad	rs199473308
Varsome	rs199473308
LitVar	rs199473308
Map	rs199473308
PheGenI	rs199473308
Biobank	rs199473308
1000 genomes	rs199473308
hgdp	rs199473308
ensembl	rs199473308
geneview	rs199473308
scholar	rs199473308
google	rs199473308
pharmgkb	rs199473308
gwascentral	rs199473308
openSNP	rs199473308
23andMe	rs199473308
SNPshot	rs199473308
SNPdbe	rs199473308
MSV3d	rs199473308
GWAS Ctlg	rs199473308

Max Magnitude

0

ClinVar
Risk	rs199473308(A;A)
Alt	rs199473308(A;A)
Reference	Rs199473308(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.38592581A>T
CLNSRC	ClinVar
CLNACC	RCV000058759.3,