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rs397515459

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515459(C;G)
Make rs397515459(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position123570979
GeneTRDN
is asnp
is mentioned by
dbSNPrs397515459
ebirs397515459
HLIrs397515459
Exacrs397515459
Varsomers397515459
Maprs397515459
PheGenIrs397515459
hapmaprs397515459
1000 genomesrs397515459
hgdprs397515459
ensemblrs397515459
gopubmedrs397515459
geneviewrs397515459
scholarrs397515459
googlers397515459
pharmgkbrs397515459
gwascentralrs397515459
openSNPrs397515459
23andMers397515459
23andMe allrs397515459
SNP Nexus

SNPshotrs397515459
SNPdbers397515459
MSV3drs397515459
GWAS Ctlgrs397515459
Max Magnitude0
ClinVar
Risk rs397515459(G,T;G,T)
Alt rs397515459(G,T;G,T)
Reference rs397515459(C;C)
Significance Pathogenic
Disease Ventricular tachycardia
Variation info
Gene TRDN
CLNDBN Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness
Reversed 1
HGVS NC_000006.11:g.123892124G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000056261.2,