rs199473162

Orientation

minus

Stabilized

minus

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

Make rs199473162(A;A)

Make rs199473162(A;T)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38586031

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473162
dbSNP (classic)	rs199473162
ClinGen	rs199473162
ebi	rs199473162
HLI	rs199473162
Exac	rs199473162
Gnomad	rs199473162
Varsome	rs199473162
LitVar	rs199473162
Map	rs199473162
PheGenI	rs199473162
Biobank	rs199473162
1000 genomes	rs199473162
hgdp	rs199473162
ensembl	rs199473162
geneview	rs199473162
scholar	rs199473162
google	rs199473162
pharmgkb	rs199473162
gwascentral	rs199473162
openSNP	rs199473162
23andMe	rs199473162
SNPshot	rs199473162
SNPdbe	rs199473162
MSV3d	rs199473162
GWAS Ctlg	rs199473162

Max Magnitude

0

ClinVar
Risk	rs199473162(A;A)
Alt	rs199473162(A;A)
Reference	Rs199473162(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.38627522A>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058502.3,