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rs794728597

From SNPedia

Orientationplus
Geno Mag Summary
(AAG;AAG) 0 common in clinvar
Make rs794728597(-;-)
Make rs794728597(-;AAG)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156130627
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728597
ebirs794728597
HLIrs794728597
Exacrs794728597
Varsomers794728597
Maprs794728597
PheGenIrs794728597
hapmaprs794728597
1000 genomesrs794728597
hgdprs794728597
ensemblrs794728597
gopubmedrs794728597
geneviewrs794728597
scholarrs794728597
googlers794728597
pharmgkbrs794728597
gwascentralrs794728597
openSNPrs794728597
23andMers794728597
23andMe allrs794728597
SNP Nexus

SNPshotrs794728597
SNPdbers794728597
MSV3drs794728597
GWAS Ctlgrs794728597
Max Magnitude0
ClinVar
Risk rs794728597(;)
Alt rs794728597(;)
Reference rs794728597(AAG;AAG)
Significance Probable-Pathogenic
Disease not provided Primary dilated cardiomyopathy
Variation info
Gene LMNA
CLNDBN not provided Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.156100418_156100420delAAG
CLNSRC
CLNACC RCV000182374.2, RCV000208440.1,