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rs869025399

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025399(-;-)
Make rs869025399(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position7582987
GeneDSP
is asnp
is mentioned by
dbSNPrs869025399
ebirs869025399
HLIrs869025399
Exacrs869025399
Varsomers869025399
Maprs869025399
PheGenIrs869025399
hapmaprs869025399
1000 genomesrs869025399
hgdprs869025399
ensemblrs869025399
gopubmedrs869025399
geneviewrs869025399
scholarrs869025399
googlers869025399
pharmgkbrs869025399
gwascentralrs869025399
openSNPrs869025399
23andMers869025399
23andMe allrs869025399
SNP Nexus

SNPshotrs869025399
SNPdbers869025399
MSV3drs869025399
GWAS Ctlgrs869025399
Max Magnitude0
ClinVar
Risk rs869025399(;)
Alt rs869025399(;)
Reference rs869025399(A;A)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene DSP
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000006.11:g.7583220delA
CLNSRC
CLNACC RCV000208031.1,