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rs397515458

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515458(C;T)
Make rs397515458(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position123503899
GeneTRDN
is asnp
is mentioned by
dbSNPrs397515458
ebirs397515458
HLIrs397515458
Exacrs397515458
Varsomers397515458
Maprs397515458
PheGenIrs397515458
hapmaprs397515458
1000 genomesrs397515458
hgdprs397515458
ensemblrs397515458
gopubmedrs397515458
geneviewrs397515458
scholarrs397515458
googlers397515458
pharmgkbrs397515458
gwascentralrs397515458
openSNPrs397515458
23andMers397515458
23andMe allrs397515458
SNP Nexus

SNPshotrs397515458
SNPdbers397515458
MSV3drs397515458
GWAS Ctlgrs397515458
Max Magnitude0
ClinVar
Risk rs397515458(T;T)
Alt rs397515458(T;T)
Reference rs397515458(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.123825044G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000056260.3,