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rs145476705

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs145476705(A;T)
Make rs145476705(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position31087781
GeneDSC2
is asnp
is mentioned by
dbSNPrs145476705
ebirs145476705
HLIrs145476705
Exacrs145476705
Varsomers145476705
Maprs145476705
PheGenIrs145476705
hapmaprs145476705
1000 genomesrs145476705
hgdprs145476705
ensemblrs145476705
gopubmedrs145476705
geneviewrs145476705
scholarrs145476705
googlers145476705
pharmgkbrs145476705
gwascentralrs145476705
openSNPrs145476705
23andMers145476705
23andMe allrs145476705
SNP Nexus

SNPshotrs145476705
SNPdbers145476705
MSV3drs145476705
GWAS Ctlgrs145476705
Max Magnitude0
ClinVar
Risk rs145476705(G,T;G,T)
Alt rs145476705(G,T;G,T)
Reference rs145476705(A;A)
Significance Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy not provided
Variation info
Gene DSC2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy not provided
Reversed 0
HGVS NC_000018.9:g.28667744A>T
CLNSRC
CLNACC RCV000149890.1, RCV000181141.1,