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rs58978449

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAG;AAG) 0 common in clinvar
Make rs58978449(-;-)
Make rs58978449(-;AAG)
ReferenceGRCh38 38.1/141
Chromosome1
Position156134946
GeneLMNA
is asnp
is mentioned by
dbSNPrs58978449
ebirs58978449
HLIrs58978449
Exacrs58978449
Varsomers58978449
Maprs58978449
PheGenIrs58978449
hapmaprs58978449
1000 genomesrs58978449
hgdprs58978449
ensemblrs58978449
gopubmedrs58978449
geneviewrs58978449
scholarrs58978449
googlers58978449
pharmgkbrs58978449
gwascentralrs58978449
openSNPrs58978449
23andMers58978449
23andMe allrs58978449
SNP Nexus

SNPshotrs58978449
SNPdbers58978449
MSV3drs58978449
GWAS Ctlgrs58978449
Max Magnitude0
ClinVar
Risk rs58978449(;)
Alt rs58978449(;)
Reference rs58978449(AAG;AAG)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy not provided
Variation info
Gene LMNA
CLNDBN Primary dilated cardiomyopathy not provided
Reversed 0
HGVS NC_000001.10:g.156104737_156104739delAAG
CLNSRC ClinVar Epithelial Biology
CLNACC RCV000041365.2, RCV000057458.1,