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rs794728589

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728589(A;A)
Make rs794728589(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156115275
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728589
ebirs794728589
HLIrs794728589
Exacrs794728589
Varsomers794728589
Maprs794728589
PheGenIrs794728589
hapmaprs794728589
1000 genomesrs794728589
hgdprs794728589
ensemblrs794728589
gopubmedrs794728589
geneviewrs794728589
scholarrs794728589
googlers794728589
pharmgkbrs794728589
gwascentralrs794728589
openSNPrs794728589
23andMers794728589
23andMe allrs794728589
SNP Nexus

SNPshotrs794728589
SNPdbers794728589
MSV3drs794728589
GWAS Ctlgrs794728589
Max Magnitude0
ClinVar
Risk rs794728589(A,C;A,C)
Alt rs794728589(A,C;A,C)
Reference rs794728589(G;G)
Significance Pathogenic
Disease not provided Primary dilated cardiomyopathy
Variation info
Gene LMNA
CLNDBN not provided Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.156085066G>A; NC_000001.10:g.156085066G>C
CLNSRC
CLNACC RCV000182355.2, RCV000218409.1,