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rs730880347

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730880347(-;-)
Make rs730880347(-;G)
Make rs730880347(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position31536265
GeneDSG2
is asnp
is mentioned by
dbSNPrs730880347
ebirs730880347
HLIrs730880347
Exacrs730880347
Varsomers730880347
Maprs730880347
PheGenIrs730880347
hapmaprs730880347
1000 genomesrs730880347
hgdprs730880347
ensemblrs730880347
gopubmedrs730880347
geneviewrs730880347
scholarrs730880347
googlers730880347
pharmgkbrs730880347
gwascentralrs730880347
openSNPrs730880347
23andMers730880347
23andMe allrs730880347
SNP Nexus

SNPshotrs730880347
SNPdbers730880347
MSV3drs730880347
GWAS Ctlgrs730880347
Max Magnitude0
ClinVar
Risk rs730880347(G;G)
Alt rs730880347(G;G)
Reference rs730880347(;)
Significance Probable-Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene DSG2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy
Reversed 0
HGVS NC_000018.9:g.29116228dupG
CLNSRC
CLNACC RCV000155624.2,