rs189125299

Orientation

plus

Stabilized

plus

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

Make rs189125299(C;T)

Make rs189125299(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

123279055

Gene

TRDN

is a	snp
is	mentioned by
dbSNP	rs189125299
dbSNP (classic)	rs189125299
ClinGen	rs189125299
ebi	rs189125299
HLI	rs189125299
Exac	rs189125299
Gnomad	rs189125299
Varsome	rs189125299
LitVar	rs189125299
Map	rs189125299
PheGenI	rs189125299
Biobank	rs189125299
1000 genomes	rs189125299
hgdp	rs189125299
ensembl	rs189125299
geneview	rs189125299
scholar	rs189125299
google	rs189125299
pharmgkb	rs189125299
gwascentral	rs189125299
openSNP	rs189125299
23andMe	rs189125299
SNPshot	rs189125299
SNPdbe	rs189125299
MSV3d	rs189125299
GWAS Ctlg	rs189125299

Max Magnitude

0

ClinVar
Risk	rs189125299(T;T)
Alt	rs189125299(T;T)
Reference	Rs189125299(C;C)
Significance	Probable-Pathogenic
Disease	Catecholaminergic polymorphic ventricular tachycardia
Variation	info
Gene	TRDN
CLNDBN	Catecholaminergic polymorphic ventricular tachycardia
Reversed	0
HGVS	NC_000006.11:g.123600200C>T
CLNSRC
CLNACC	RCV000458621.1,