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rs193298428

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193298428(A;C)
Make rs193298428(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31536259
GeneDSG2
is asnp
is mentioned by
dbSNPrs193298428
ebirs193298428
HLIrs193298428
Exacrs193298428
Varsomers193298428
Maprs193298428
PheGenIrs193298428
hapmaprs193298428
1000 genomesrs193298428
hgdprs193298428
ensemblrs193298428
gopubmedrs193298428
geneviewrs193298428
scholarrs193298428
googlers193298428
pharmgkbrs193298428
gwascentralrs193298428
openSNPrs193298428
23andMers193298428
23andMe allrs193298428
SNP Nexus

SNPshotrs193298428
SNPdbers193298428
MSV3drs193298428
GWAS Ctlgrs193298428
Max Magnitude0
ClinVar
Risk rs193298428(C;C)
Alt rs193298428(C;C)
Reference rs193298428(A;A)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene DSG2
CLNDBN Cardiomyopathy
Reversed 0
HGVS NC_000018.9:g.29116222A>C
CLNSRC
CLNACC RCV000181219.1,