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rs1060500613

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060500613(-;-)
Make rs1060500613(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position7571564
GeneDSP
is asnp
is mentioned by
dbSNPrs1060500613
dbSNP (old)rs1060500613
ClinGenrs1060500613
ebirs1060500613
HLIrs1060500613
Exacrs1060500613
Gnomadrs1060500613
Varsomers1060500613
LitVarrs1060500613
Maprs1060500613
PheGenIrs1060500613
Biobankrs1060500613
1000 genomesrs1060500613
hgdprs1060500613
ensemblrs1060500613
gopubmedrs1060500613
geneviewrs1060500613
scholarrs1060500613
googlers1060500613
pharmgkbrs1060500613
gwascentralrs1060500613
openSNPrs1060500613
23andMers1060500613
23andMe allrs1060500613
SNPshotrs1060500613
SNPdbers1060500613
MSV3drs1060500613
GWAS Ctlgrs1060500613
Max Magnitude0
ClinVar
Risk rs1060500613(-;-)
Alt rs1060500613(-;-)
Reference Rs1060500613(G;G)
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.7571797delG
CLNSRC
CLNACC RCV000468365.1,