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rs377272752

From SNPedia

Orientationplus
Geno Mag Summary
(TCC;TCC) 0 common in clinvar
Make rs377272752(-;-)
Make rs377272752(-;CCT)
Make rs377272752(CCT;CCT)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position31069032
GeneDSC2
is asnp
is mentioned by
dbSNPrs377272752
ebirs377272752
HLIrs377272752
Exacrs377272752
Varsomers377272752
Maprs377272752
PheGenIrs377272752
hapmaprs377272752
1000 genomesrs377272752
hgdprs377272752
ensemblrs377272752
gopubmedrs377272752
geneviewrs377272752
scholarrs377272752
googlers377272752
pharmgkbrs377272752
gwascentralrs377272752
openSNPrs377272752
23andMers377272752
23andMe allrs377272752
SNP Nexus

SNPshotrs377272752
SNPdbers377272752
MSV3drs377272752
GWAS Ctlgrs377272752
Max Magnitude0
ClinVar
Risk rs377272752(;)
Alt rs377272752(;)
Reference rs377272752(TCC;TCC)
Significance Probable-Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy Cardiomyopathy
Variation info
Gene DSC2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy Cardiomyopathy
Reversed 0
HGVS NC_000018.9:g.28648998_28649000delTCC
CLNSRC
CLNACC RCV000157177.1, RCV000181173.1,