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rs397517887

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATGGAGATCCACGCC;ATGGAGATCCACGCC) 0 common in clinvar
(CATGGAGATCCACGC;CATGGAGATCCACGC) 0 common in clinvar
Make rs397517887(-;-)
Make rs397517887(-;ATGGAGATCCACGCC)
ReferenceGRCh38 38.1/141
Chromosome1
Position156136075
GeneLMNA
is asnp
is mentioned by
dbSNPrs397517887
dbSNP (old)rs397517887
ClinGenrs397517887
ebirs397517887
HLIrs397517887
Exacrs397517887
Varsomers397517887
Maprs397517887
PheGenIrs397517887
Biobankrs397517887
1000 genomesrs397517887
hgdprs397517887
ensemblrs397517887
gopubmedrs397517887
geneviewrs397517887
scholarrs397517887
googlers397517887
pharmgkbrs397517887
gwascentralrs397517887
openSNPrs397517887
23andMers397517887
23andMe allrs397517887
SNP Nexus

SNPshotrs397517887
SNPdbers397517887
MSV3drs397517887
GWAS Ctlgrs397517887
Max Magnitude0
ClinVar
Risk rs397517887(-;-)
Alt rs397517887(-;-)
Reference Rs397517887(CATGGAGATCCACGC;CATGGAGATCCACGC)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene LMNA
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.156105866_156105880delATGGAGATCCACGCC
CLNSRC ClinVar
CLNACC RCV000041306.2,