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rs869025388

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025388(A;A)
Make rs869025388(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome18
Position31524549
GeneDSG2
is asnp
is mentioned by
dbSNPrs869025388
ebirs869025388
HLIrs869025388
Exacrs869025388
Varsomers869025388
Maprs869025388
PheGenIrs869025388
hapmaprs869025388
1000 genomesrs869025388
hgdprs869025388
ensemblrs869025388
gopubmedrs869025388
geneviewrs869025388
scholarrs869025388
googlers869025388
pharmgkbrs869025388
gwascentralrs869025388
openSNPrs869025388
23andMers869025388
23andMe allrs869025388
SNP Nexus

SNPshotrs869025388
SNPdbers869025388
MSV3drs869025388
GWAS Ctlgrs869025388
Max Magnitude0
ClinVar
Risk rs869025388(A;A)
Alt rs869025388(A;A)
Reference rs869025388(T;T)
Significance Probable-Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene DSG2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy
Reversed 0
HGVS NC_000018.9:g.29104512T>A
CLNSRC
CLNACC RCV000208038.1,