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rs1060500618

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060500618(C;T)
Make rs1060500618(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position7575460
GeneDSP
is asnp
is mentioned by
dbSNPrs1060500618
dbSNP (old)rs1060500618
ClinGenrs1060500618
ebirs1060500618
HLIrs1060500618
Exacrs1060500618
Gnomadrs1060500618
Varsomers1060500618
Maprs1060500618
PheGenIrs1060500618
Biobankrs1060500618
1000 genomesrs1060500618
hgdprs1060500618
ensemblrs1060500618
gopubmedrs1060500618
geneviewrs1060500618
scholarrs1060500618
googlers1060500618
pharmgkbrs1060500618
gwascentralrs1060500618
openSNPrs1060500618
23andMers1060500618
23andMe allrs1060500618
SNPshotrs1060500618
SNPdbers1060500618
MSV3drs1060500618
GWAS Ctlgrs1060500618
Max Magnitude0
ClinVar
Risk rs1060500618(T;T)
Alt rs1060500618(T;T)
Reference Rs1060500618(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.7575693C>T
CLNSRC
CLNACC RCV000460155.1,