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rs752432726

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs752432726(A;G)
Make rs752432726(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31524754
GeneDSG2
is asnp
is mentioned by
dbSNPrs752432726
ebirs752432726
HLIrs752432726
Exacrs752432726
Varsomers752432726
Maprs752432726
PheGenIrs752432726
hapmaprs752432726
1000 genomesrs752432726
hgdprs752432726
ensemblrs752432726
gopubmedrs752432726
geneviewrs752432726
scholarrs752432726
googlers752432726
pharmgkbrs752432726
gwascentralrs752432726
openSNPrs752432726
23andMers752432726
23andMe allrs752432726
SNP Nexus

SNPshotrs752432726
SNPdbers752432726
MSV3drs752432726
GWAS Ctlgrs752432726
Max Magnitude0
ClinVar
Risk rs752432726(G;G)
Alt rs752432726(G;G)
Reference rs752432726(A;A)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene DSG2
CLNDBN Cardiomyopathy
Reversed 0
HGVS NC_000018.9:g.29104717A>G
CLNSRC
CLNACC RCV000181211.1,