Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1060502114

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502114(-;-)
Make rs1060502114(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position123503894
GeneTRDN
is asnp
is mentioned by
dbSNPrs1060502114
dbSNP (old)rs1060502114
ClinGenrs1060502114
ebirs1060502114
HLIrs1060502114
Exacrs1060502114
Gnomadrs1060502114
Varsomers1060502114
Maprs1060502114
PheGenIrs1060502114
Biobankrs1060502114
1000 genomesrs1060502114
hgdprs1060502114
ensemblrs1060502114
gopubmedrs1060502114
geneviewrs1060502114
scholarrs1060502114
googlers1060502114
pharmgkbrs1060502114
gwascentralrs1060502114
openSNPrs1060502114
23andMers1060502114
23andMe allrs1060502114
SNPshotrs1060502114
SNPdbers1060502114
MSV3drs1060502114
GWAS Ctlgrs1060502114
Max Magnitude0
ClinVar
Risk rs1060502114(-;-)
Alt rs1060502114(-;-)
Reference Rs1060502114(G;G)
Significance Pathogenic
Disease Catecholaminergic polymorphic ventricular tachycardia
Variation info
Gene TRDN
CLNDBN Catecholaminergic polymorphic ventricular tachycardia
Reversed 1
HGVS NC_000006.11:g.123825039delC
CLNSRC
CLNACC RCV000468888.1,