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rs758950880

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs758950880(C;C)
Make rs758950880(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31068145
GeneDSC2
is asnp
is mentioned by
dbSNPrs758950880
ebirs758950880
HLIrs758950880
Exacrs758950880
Varsomers758950880
Maprs758950880
PheGenIrs758950880
hapmaprs758950880
1000 genomesrs758950880
hgdprs758950880
ensemblrs758950880
gopubmedrs758950880
geneviewrs758950880
scholarrs758950880
googlers758950880
pharmgkbrs758950880
gwascentralrs758950880
openSNPrs758950880
23andMers758950880
23andMe allrs758950880
SNP Nexus

SNPshotrs758950880
SNPdbers758950880
MSV3drs758950880
GWAS Ctlgrs758950880
Max Magnitude0
ClinVar
Risk rs758950880(C;C)
Alt rs758950880(C;C)
Reference rs758950880(T;T)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene DSC2
CLNDBN Cardiomyopathy
Reversed 0
HGVS NC_000018.9:g.28648111T>C
CLNSRC
CLNACC RCV000181180.1,