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rs758537946

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs758537946(A;A)
Make rs758537946(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31531044
GeneDSG2
is asnp
is mentioned by
dbSNPrs758537946
ebirs758537946
HLIrs758537946
Exacrs758537946
Varsomers758537946
Maprs758537946
PheGenIrs758537946
hapmaprs758537946
1000 genomesrs758537946
hgdprs758537946
ensemblrs758537946
gopubmedrs758537946
geneviewrs758537946
scholarrs758537946
googlers758537946
pharmgkbrs758537946
gwascentralrs758537946
openSNPrs758537946
23andMers758537946
23andMe allrs758537946
SNP Nexus

SNPshotrs758537946
SNPdbers758537946
MSV3drs758537946
GWAS Ctlgrs758537946
Max Magnitude0
ClinVar
Risk rs758537946(A;A)
Alt rs758537946(A;A)
Reference rs758537946(G;G)
Significance Probable-Pathogenic
Disease not specified Primary dilated cardiomyopathy
Variation info
Gene DSG2
CLNDBN not specified Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000018.9:g.29111007G>A
CLNSRC
CLNACC RCV000181214.2, RCV000208418.1,