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rs587782956

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587782956(-;-)
Make rs587782956(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156136050
GeneLMNA
is asnp
is mentioned by
dbSNPrs587782956
ebirs587782956
HLIrs587782956
Exacrs587782956
Varsomers587782956
Maprs587782956
PheGenIrs587782956
hapmaprs587782956
1000 genomesrs587782956
hgdprs587782956
ensemblrs587782956
gopubmedrs587782956
geneviewrs587782956
scholarrs587782956
googlers587782956
pharmgkbrs587782956
gwascentralrs587782956
openSNPrs587782956
23andMers587782956
23andMe allrs587782956
SNP Nexus

SNPshotrs587782956
SNPdbers587782956
MSV3drs587782956
GWAS Ctlgrs587782956
Max Magnitude0
ClinVar
Risk rs587782956(;)
Alt rs587782956(;)
Reference rs587782956(T;T)
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.156105841delT
CLNSRC
CLNACC RCV000057230.1, RCV000143910.1,