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rs201564919

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201564919(A;A)
Make rs201564919(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31541225
GeneDSG2
is asnp
is mentioned by
dbSNPrs201564919
ebirs201564919
HLIrs201564919
Exacrs201564919
Varsomers201564919
Maprs201564919
PheGenIrs201564919
hapmaprs201564919
1000 genomesrs201564919
hgdprs201564919
ensemblrs201564919
gopubmedrs201564919
geneviewrs201564919
scholarrs201564919
googlers201564919
pharmgkbrs201564919
gwascentralrs201564919
openSNPrs201564919
23andMers201564919
23andMe allrs201564919
SNP Nexus

SNPshotrs201564919
SNPdbers201564919
MSV3drs201564919
GWAS Ctlgrs201564919
Max Magnitude0
ClinVar
Risk rs201564919(A;A)
Alt rs201564919(A;A)
Reference rs201564919(G;G)
Significance Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy not specified
Variation info
Gene DSG2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy not specified
Reversed 0
HGVS NC_000018.9:g.29121188G>A
CLNSRC
CLNACC RCV000148474.1, RCV000154703.1,