Have questions? Visit https://www.reddit.com/r/SNPedia

rs397517915

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517915(-;-)
Make rs397517915(-;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position156135922
GeneLMNA
is asnp
is mentioned by
dbSNPrs397517915
ebirs397517915
HLIrs397517915
Exacrs397517915
Varsomers397517915
Maprs397517915
PheGenIrs397517915
hapmaprs397517915
1000 genomesrs397517915
hgdprs397517915
ensemblrs397517915
gopubmedrs397517915
geneviewrs397517915
scholarrs397517915
googlers397517915
pharmgkbrs397517915
gwascentralrs397517915
openSNPrs397517915
23andMers397517915
23andMe allrs397517915
SNP Nexus

SNPshotrs397517915
SNPdbers397517915
MSV3drs397517915
GWAS Ctlgrs397517915
Max Magnitude0
ClinVar
Risk rs397517915(;)
Alt rs397517915(;)
Reference rs397517915(C;C)
Significance Pathogenic
Disease Primary dilated cardiomyopathy not provided
Variation info
Gene LMNA
CLNDBN Primary dilated cardiomyopathy not provided
Reversed 0
HGVS NC_000001.10:g.156105713delC
CLNSRC ClinVar
CLNACC RCV000041381.2, RCV000236709.1,