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rs397517895

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517895(C;G)
Make rs397517895(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position156115072
GeneLMNA
is asnp
is mentioned by
dbSNPrs397517895
ebirs397517895
HLIrs397517895
Exacrs397517895
Varsomers397517895
Maprs397517895
PheGenIrs397517895
hapmaprs397517895
1000 genomesrs397517895
hgdprs397517895
ensemblrs397517895
gopubmedrs397517895
geneviewrs397517895
scholarrs397517895
googlers397517895
pharmgkbrs397517895
gwascentralrs397517895
openSNPrs397517895
23andMers397517895
23andMe allrs397517895
SNP Nexus

SNPshotrs397517895
SNPdbers397517895
MSV3drs397517895
GWAS Ctlgrs397517895
Max Magnitude0
ClinVar
Risk rs397517895(G;G)
Alt rs397517895(G;G)
Reference rs397517895(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene LMNA
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.156084863C>G
CLNSRC ClinVar
CLNACC RCV000041321.2,