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rs869025392

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025392(A;A)
Make rs869025392(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position7580993
GeneDSP
is asnp
is mentioned by
dbSNPrs869025392
ebirs869025392
HLIrs869025392
Exacrs869025392
Varsomers869025392
Maprs869025392
PheGenIrs869025392
hapmaprs869025392
1000 genomesrs869025392
hgdprs869025392
ensemblrs869025392
gopubmedrs869025392
geneviewrs869025392
scholarrs869025392
googlers869025392
pharmgkbrs869025392
gwascentralrs869025392
openSNPrs869025392
23andMers869025392
23andMe allrs869025392
SNP Nexus

SNPshotrs869025392
SNPdbers869025392
MSV3drs869025392
GWAS Ctlgrs869025392
Max Magnitude0
ClinVar
Risk rs869025392(A;A)
Alt rs869025392(A;A)
Reference rs869025392(G;G)
Significance Probable-Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene DSP
CLNDBN Arrhythmogenic right ventricular cardiomyopathy
Reversed 0
HGVS NC_000006.11:g.7581226G>A
CLNSRC
CLNACC RCV000208438.1,