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rs794728591

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728591(C;T)
Make rs794728591(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156134811
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728591
ebirs794728591
HLIrs794728591
Exacrs794728591
Varsomers794728591
Maprs794728591
PheGenIrs794728591
hapmaprs794728591
1000 genomesrs794728591
hgdprs794728591
ensemblrs794728591
gopubmedrs794728591
geneviewrs794728591
scholarrs794728591
googlers794728591
pharmgkbrs794728591
gwascentralrs794728591
openSNPrs794728591
23andMers794728591
23andMe allrs794728591
SNP Nexus

SNPshotrs794728591
SNPdbers794728591
MSV3drs794728591
GWAS Ctlgrs794728591
Max Magnitude0
ClinVar
Risk rs794728591(T;T)
Alt rs794728591(T;T)
Reference rs794728591(C;C)
Significance Probable-Pathogenic
Disease not specified Primary dilated cardiomyopathy
Variation info
Gene LMNA
CLNDBN not specified Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.156104602C>T
CLNSRC
CLNACC RCV000182360.3, RCV000208531.1,