rs397515458

Orientation

minus

Stabilized

minus

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

Make rs397515458(C;T)

Make rs397515458(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

123503899

Gene

TRDN

is a	snp
is	mentioned by
dbSNP	rs397515458
dbSNP (classic)	rs397515458
ClinGen	rs397515458
ebi	rs397515458
HLI	rs397515458
Exac	rs397515458
Gnomad	rs397515458
Varsome	rs397515458
LitVar	rs397515458
Map	rs397515458
PheGenI	rs397515458
Biobank	rs397515458
1000 genomes	rs397515458
hgdp	rs397515458
ensembl	rs397515458
geneview	rs397515458
scholar	rs397515458
google	rs397515458
pharmgkb	rs397515458
gwascentral	rs397515458
openSNP	rs397515458
23andMe	rs397515458
SNPshot	rs397515458
SNPdbe	rs397515458
MSV3d	rs397515458
GWAS Ctlg	rs397515458

Max Magnitude

0

ClinVar
Risk	rs397515458(T;T)
Alt	rs397515458(T;T)
Reference	Rs397515458(C;C)
Significance	Pathogenic
Disease	Ventricular tachycardia not provided
Variation	info
Gene	TRDN
CLNDBN	Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness not provided
Reversed	1
HGVS	NC_000006.11:g.123825044G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000056260.3, RCV000484797.1,