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rs794728593

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728593(A;A)
Make rs794728593(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position156134933
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728593
ebirs794728593
HLIrs794728593
Exacrs794728593
Varsomers794728593
Maprs794728593
PheGenIrs794728593
hapmaprs794728593
1000 genomesrs794728593
hgdprs794728593
ensemblrs794728593
gopubmedrs794728593
geneviewrs794728593
scholarrs794728593
googlers794728593
pharmgkbrs794728593
gwascentralrs794728593
openSNPrs794728593
23andMers794728593
23andMe allrs794728593
SNP Nexus

SNPshotrs794728593
SNPdbers794728593
MSV3drs794728593
GWAS Ctlgrs794728593
Max Magnitude0
ClinVar
Risk rs794728593(A;A)
Alt rs794728593(A;A)
Reference rs794728593(G;G)
Significance Pathogenic
Disease not specified Primary dilated cardiomyopathy
Variation info
Gene LMNA
CLNDBN not specified Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.156104724G>A
CLNSRC
CLNACC RCV000182364.2, RCV000219229.1,