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rs587782927

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs587782927(-;-)
Make rs587782927(-;AG)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position7574086
GeneDSP
is asnp
is mentioned by
dbSNPrs587782927
ebirs587782927
HLIrs587782927
Exacrs587782927
Varsomers587782927
Maprs587782927
PheGenIrs587782927
hapmaprs587782927
1000 genomesrs587782927
hgdprs587782927
ensemblrs587782927
gopubmedrs587782927
geneviewrs587782927
scholarrs587782927
googlers587782927
pharmgkbrs587782927
gwascentralrs587782927
openSNPrs587782927
23andMers587782927
23andMe allrs587782927
SNP Nexus

SNPshotrs587782927
SNPdbers587782927
MSV3drs587782927
GWAS Ctlgrs587782927
Max Magnitude0
ClinVar
Risk rs587782927(;)
Alt rs587782927(;)
Reference rs587782927(AG;AG)
Significance Probable-Pathogenic
Disease Left ventricular noncompaction cardiomyopathy Ventricular tachycardia Primary dilated cardiomyopathy
Variation info
Gene DSP
CLNDBN Left ventricular noncompaction cardiomyopathy Ventricular tachycardia Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000006.11:g.7574319_7574320delAG
CLNSRC
CLNACC RCV000133469.1, RCV000143886.1,