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rs878853170

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853170(C;T)
Make rs878853170(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome18
Position31079850
GeneDSC2
is asnp
is mentioned by
dbSNPrs878853170
ebirs878853170
HLIrs878853170
Exacrs878853170
Varsomers878853170
Maprs878853170
PheGenIrs878853170
hapmaprs878853170
1000 genomesrs878853170
hgdprs878853170
ensemblrs878853170
gopubmedrs878853170
geneviewrs878853170
scholarrs878853170
googlers878853170
pharmgkbrs878853170
gwascentralrs878853170
openSNPrs878853170
23andMers878853170
23andMe allrs878853170
SNP Nexus

SNPshotrs878853170
SNPdbers878853170
MSV3drs878853170
GWAS Ctlgrs878853170
Max Magnitude0
ClinVar
Risk rs878853170(T;T)
Alt rs878853170(T;T)
Reference rs878853170(C;C)
Significance Pathogenic
Disease ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA
Variation info
Gene DSC2
CLNDBN ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11, WITH OR WITHOUT MILD PALMOPLANTAR KERATODERMA
Reversed 1
HGVS NC_000018.9:g.28659816G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000224990.1,