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rs189125299

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs189125299(C;T)
Make rs189125299(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position123279055
GeneTRDN
is asnp
is mentioned by
dbSNPrs189125299
dbSNP (old)rs189125299
ClinGenrs189125299
ebirs189125299
HLIrs189125299
Exacrs189125299
Gnomadrs189125299
Varsomers189125299
Maprs189125299
PheGenIrs189125299
Biobankrs189125299
1000 genomesrs189125299
hgdprs189125299
ensemblrs189125299
gopubmedrs189125299
geneviewrs189125299
scholarrs189125299
googlers189125299
pharmgkbrs189125299
gwascentralrs189125299
openSNPrs189125299
23andMers189125299
23andMe allrs189125299
SNPshotrs189125299
SNPdbers189125299
MSV3drs189125299
GWAS Ctlgrs189125299
Max Magnitude0
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,