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rs397517911

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517911(C;G)
Make rs397517911(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position156135239
GeneLMNA
is asnp
is mentioned by
dbSNPrs397517911
ebirs397517911
HLIrs397517911
Exacrs397517911
Varsomers397517911
Maprs397517911
PheGenIrs397517911
hapmaprs397517911
1000 genomesrs397517911
hgdprs397517911
ensemblrs397517911
gopubmedrs397517911
geneviewrs397517911
scholarrs397517911
googlers397517911
pharmgkbrs397517911
gwascentralrs397517911
openSNPrs397517911
23andMers397517911
23andMe allrs397517911
SNP Nexus

SNPshotrs397517911
SNPdbers397517911
MSV3drs397517911
GWAS Ctlgrs397517911
Max Magnitude0
ClinVar
Risk rs397517911(G;G)
Alt rs397517911(G;G)
Reference rs397517911(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene LMNA
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.156105030C>G
CLNSRC ClinVar
CLNACC RCV000041375.2,