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rs397517909

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517909(G;T)
Make rs397517909(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position156134949
GeneLMNA
is asnp
is mentioned by
dbSNPrs397517909
ebirs397517909
HLIrs397517909
Exacrs397517909
Varsomers397517909
Maprs397517909
PheGenIrs397517909
hapmaprs397517909
1000 genomesrs397517909
hgdprs397517909
ensemblrs397517909
gopubmedrs397517909
geneviewrs397517909
scholarrs397517909
googlers397517909
pharmgkbrs397517909
gwascentralrs397517909
openSNPrs397517909
23andMers397517909
23andMe allrs397517909
SNP Nexus

SNPshotrs397517909
SNPdbers397517909
MSV3drs397517909
GWAS Ctlgrs397517909
Max Magnitude0
ClinVar
Risk rs397517909(T;T)
Alt rs397517909(T;T)
Reference rs397517909(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene LMNA
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.156104740G>T
CLNSRC ClinVar
CLNACC RCV000041366.2,