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rs869025398

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025398(G;G)
Make rs869025398(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position7567451
GeneDSP
is asnp
is mentioned by
dbSNPrs869025398
ebirs869025398
HLIrs869025398
Exacrs869025398
Varsomers869025398
Maprs869025398
PheGenIrs869025398
hapmaprs869025398
1000 genomesrs869025398
hgdprs869025398
ensemblrs869025398
gopubmedrs869025398
geneviewrs869025398
scholarrs869025398
googlers869025398
pharmgkbrs869025398
gwascentralrs869025398
openSNPrs869025398
23andMers869025398
23andMe allrs869025398
SNP Nexus

SNPshotrs869025398
SNPdbers869025398
MSV3drs869025398
GWAS Ctlgrs869025398
Max Magnitude0
ClinVar
Risk rs869025398(G;G)
Alt rs869025398(G;G)
Reference rs869025398(T;T)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene DSP
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000006.11:g.7567684T>G
CLNSRC
CLNACC RCV000208157.1,