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rs1060500610

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060500610(C;T)
Make rs1060500610(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position7581012
GeneDSP
is asnp
is mentioned by
dbSNPrs1060500610
dbSNP (old)rs1060500610
ClinGenrs1060500610
ebirs1060500610
HLIrs1060500610
Exacrs1060500610
Gnomadrs1060500610
Varsomers1060500610
Maprs1060500610
PheGenIrs1060500610
Biobankrs1060500610
1000 genomesrs1060500610
hgdprs1060500610
ensemblrs1060500610
gopubmedrs1060500610
geneviewrs1060500610
scholarrs1060500610
googlers1060500610
pharmgkbrs1060500610
gwascentralrs1060500610
openSNPrs1060500610
23andMers1060500610
23andMe allrs1060500610
SNPshotrs1060500610
SNPdbers1060500610
MSV3drs1060500610
GWAS Ctlgrs1060500610
Max Magnitude0
ClinVar
Risk rs1060500610(T;T)
Alt rs1060500610(T;T)
Reference Rs1060500610(C;C)
Significance Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene DSP
CLNDBN Arrhythmogenic right ventricular cardiomyopathy, type 8
Reversed 0
HGVS NC_000006.11:g.7581245C>T
CLNSRC
CLNACC RCV000472826.1,