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rs397517886

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397517886(C;C)
Make rs397517886(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position156136070
GeneLMNA
is asnp
is mentioned by
dbSNPrs397517886
ebirs397517886
HLIrs397517886
Exacrs397517886
Varsomers397517886
Maprs397517886
PheGenIrs397517886
hapmaprs397517886
1000 genomesrs397517886
hgdprs397517886
ensemblrs397517886
gopubmedrs397517886
geneviewrs397517886
scholarrs397517886
googlers397517886
pharmgkbrs397517886
gwascentralrs397517886
openSNPrs397517886
23andMers397517886
23andMe allrs397517886
SNP Nexus

SNPshotrs397517886
SNPdbers397517886
MSV3drs397517886
GWAS Ctlgrs397517886
Max Magnitude0
ClinVar
Risk rs397517886(C;C)
Alt rs397517886(C;C)
Reference rs397517886(T;T)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy not specified
Variation info
Gene LMNA
CLNDBN Primary dilated cardiomyopathy not specified
Reversed 0
HGVS NC_000001.10:g.156105861T>C
CLNSRC ClinVar
CLNACC RCV000041305.2, RCV000236658.1,