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rs397516956

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397516956(-;-)
Make rs397516956(-;A)
Make rs397516956(A;A)
ReferenceGRCh38 38.1/141
Chromosome6
Position7562766
GeneDSP
is asnp
is mentioned by
dbSNPrs397516956
ebirs397516956
HLIrs397516956
Exacrs397516956
Varsomers397516956
Maprs397516956
PheGenIrs397516956
hapmaprs397516956
1000 genomesrs397516956
hgdprs397516956
ensemblrs397516956
gopubmedrs397516956
geneviewrs397516956
scholarrs397516956
googlers397516956
pharmgkbrs397516956
gwascentralrs397516956
openSNPrs397516956
23andMers397516956
23andMe allrs397516956
SNP Nexus

SNPshotrs397516956
SNPdbers397516956
MSV3drs397516956
GWAS Ctlgrs397516956
Max Magnitude0
ClinVar
Risk rs397516956(A;A)
Alt rs397516956(A;A)
Reference rs397516956(;)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene DSP
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000006.11:g.7562999dupA
CLNSRC ClinVar
CLNACC RCV000038084.2,