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rs869025395

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025395(C;T)
Make rs869025395(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position7583113
GeneDSP
is asnp
is mentioned by
dbSNPrs869025395
ebirs869025395
HLIrs869025395
Exacrs869025395
Varsomers869025395
Maprs869025395
PheGenIrs869025395
hapmaprs869025395
1000 genomesrs869025395
hgdprs869025395
ensemblrs869025395
gopubmedrs869025395
geneviewrs869025395
scholarrs869025395
googlers869025395
pharmgkbrs869025395
gwascentralrs869025395
openSNPrs869025395
23andMers869025395
23andMe allrs869025395
SNP Nexus

SNPshotrs869025395
SNPdbers869025395
MSV3drs869025395
GWAS Ctlgrs869025395
Max Magnitude0
ClinVar
Risk rs869025395(T;T)
Alt rs869025395(T;T)
Reference rs869025395(C;C)
Significance Probable-Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene DSP
CLNDBN Arrhythmogenic right ventricular cardiomyopathy
Reversed 0
HGVS NC_000006.11:g.7583346C>T
CLNSRC
CLNACC RCV000208287.1,