rs199473107

Orientation

minus

Stabilized

minus

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

Make rs199473107(A;A)

Make rs199473107(A;T)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38606078

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473107
dbSNP (classic)	rs199473107
ClinGen	rs199473107
ebi	rs199473107
HLI	rs199473107
Exac	rs199473107
Gnomad	rs199473107
Varsome	rs199473107
LitVar	rs199473107
Map	rs199473107
PheGenI	rs199473107
Biobank	rs199473107
1000 genomes	rs199473107
hgdp	rs199473107
ensembl	rs199473107
geneview	rs199473107
scholar	rs199473107
google	rs199473107
pharmgkb	rs199473107
gwascentral	rs199473107
openSNP	rs199473107
23andMe	rs199473107
SNPshot	rs199473107
SNPdbe	rs199473107
MSV3d	rs199473107
GWAS Ctlg	rs199473107

Max Magnitude

0

ClinVar
Risk	rs199473107(A;A)
Alt	rs199473107(A;A)
Reference	Rs199473107(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.38647569A>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058403.3,