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rs397517908

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517908(-;-)
Make rs397517908(-;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position156134928
GeneLMNA
is asnp
is mentioned by
dbSNPrs397517908
ebirs397517908
HLIrs397517908
Exacrs397517908
Varsomers397517908
Maprs397517908
PheGenIrs397517908
hapmaprs397517908
1000 genomesrs397517908
hgdprs397517908
ensemblrs397517908
gopubmedrs397517908
geneviewrs397517908
scholarrs397517908
googlers397517908
pharmgkbrs397517908
gwascentralrs397517908
openSNPrs397517908
23andMers397517908
23andMe allrs397517908
SNP Nexus

SNPshotrs397517908
SNPdbers397517908
MSV3drs397517908
GWAS Ctlgrs397517908
Max Magnitude0
ClinVar
Risk rs397517908(;)
Alt rs397517908(;)
Reference rs397517908(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene LMNA
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.156104719delC
CLNSRC ClinVar
CLNACC RCV000041364.2,