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rs397516945

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs397516945(-;A)
Make rs397516945(A;A)
ReferenceGRCh38 38.1/141
Chromosome6
Position7559337
GeneDSP
is asnp
is mentioned by
dbSNPrs397516945
dbSNP (classic)rs397516945
ClinGenrs397516945
ebirs397516945
HLIrs397516945
Exacrs397516945
Gnomadrs397516945
Varsomers397516945
LitVarrs397516945
Maprs397516945
PheGenIrs397516945
Biobankrs397516945
1000 genomesrs397516945
hgdprs397516945
ensemblrs397516945
geneviewrs397516945
scholarrs397516945
googlers397516945
pharmgkbrs397516945
gwascentralrs397516945
openSNPrs397516945
23andMers397516945
SNPshotrs397516945
SNPdbers397516945
MSV3drs397516945
GWAS Ctlgrs397516945
Max Magnitude0
ClinVar
Risk rs397516945(A;A)
Alt rs397516945(A;A)
Reference Rs397516945(;)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene DSP
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000006.11:g.7559570_7559571insA
CLNSRC ClinVar
CLNACC RCV000038063.2,