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rs794728608

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728608(-;-)
Make rs794728608(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156135235
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728608
ebirs794728608
HLIrs794728608
Exacrs794728608
Varsomers794728608
Maprs794728608
PheGenIrs794728608
hapmaprs794728608
1000 genomesrs794728608
hgdprs794728608
ensemblrs794728608
gopubmedrs794728608
geneviewrs794728608
scholarrs794728608
googlers794728608
pharmgkbrs794728608
gwascentralrs794728608
openSNPrs794728608
23andMers794728608
23andMe allrs794728608
SNP Nexus

SNPshotrs794728608
SNPdbers794728608
MSV3drs794728608
GWAS Ctlgrs794728608
Max Magnitude0
ClinVar
Risk rs794728608(;)
Alt rs794728608(;)
Reference rs794728608(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.156105026delG
CLNSRC
CLNACC RCV000182389.1, RCV000208368.1,