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rs794729075

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729075(A;A)
Make rs794729075(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position68197426
GeneMYPN
is asnp
is mentioned by
dbSNPrs794729075
ebirs794729075
HLIrs794729075
Exacrs794729075
Varsomers794729075
Maprs794729075
PheGenIrs794729075
hapmaprs794729075
1000 genomesrs794729075
hgdprs794729075
ensemblrs794729075
gopubmedrs794729075
geneviewrs794729075
scholarrs794729075
googlers794729075
pharmgkbrs794729075
gwascentralrs794729075
openSNPrs794729075
23andMers794729075
23andMe allrs794729075
SNP Nexus

SNPshotrs794729075
SNPdbers794729075
MSV3drs794729075
GWAS Ctlgrs794729075
Max Magnitude0
ClinVar
Risk rs794729075(A;A)
Alt rs794729075(A;A)
Reference rs794729075(C;C)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYPN
CLNDBN Cardiomyopathy
Reversed 0
HGVS NC_000010.10:g.69957183C>A
CLNSRC
CLNACC RCV000183594.1,