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rs397517893

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397517893(A;G)
Make rs397517893(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position156136982
GeneLMNA
is asnp
is mentioned by
dbSNPrs397517893
ebirs397517893
HLIrs397517893
Exacrs397517893
Varsomers397517893
Maprs397517893
PheGenIrs397517893
hapmaprs397517893
1000 genomesrs397517893
hgdprs397517893
ensemblrs397517893
gopubmedrs397517893
geneviewrs397517893
scholarrs397517893
googlers397517893
pharmgkbrs397517893
gwascentralrs397517893
openSNPrs397517893
23andMers397517893
23andMe allrs397517893
SNP Nexus

SNPshotrs397517893
SNPdbers397517893
MSV3drs397517893
GWAS Ctlgrs397517893
Max Magnitude0
ClinVar
Risk rs397517893(G;G)
Alt rs397517893(G;G)
Reference rs397517893(A;A)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene LMNA
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.156106773A>G
CLNSRC ClinVar
CLNACC RCV000041317.2,