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rs1060500609

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060500609(G;T)
Make rs1060500609(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position7569185
GeneDSP
is asnp
is mentioned by
dbSNPrs1060500609
dbSNP (old)rs1060500609
ClinGenrs1060500609
ebirs1060500609
HLIrs1060500609
Exacrs1060500609
Gnomadrs1060500609
Varsomers1060500609
Maprs1060500609
PheGenIrs1060500609
Biobankrs1060500609
1000 genomesrs1060500609
hgdprs1060500609
ensemblrs1060500609
gopubmedrs1060500609
geneviewrs1060500609
scholarrs1060500609
googlers1060500609
pharmgkbrs1060500609
gwascentralrs1060500609
openSNPrs1060500609
23andMers1060500609
23andMe allrs1060500609
SNPshotrs1060500609
SNPdbers1060500609
MSV3drs1060500609
GWAS Ctlgrs1060500609
Max Magnitude0
ClinVar
Risk rs1060500609(T;T)
Alt rs1060500609(T;T)
Reference Rs1060500609(G;G)
Significance Probable-Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene DSP
CLNDBN Arrhythmogenic right ventricular cardiomyopathy, type 8
Reversed 0
HGVS NC_000006.11:g.7569418G>T
CLNSRC
CLNACC RCV000465188.1,