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rs267607646

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267607646(-;-)
Make rs267607646(-;G)
Make rs267607646(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position156115266
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607646
ebirs267607646
HLIrs267607646
Exacrs267607646
Varsomers267607646
Maprs267607646
PheGenIrs267607646
hapmaprs267607646
1000 genomesrs267607646
hgdprs267607646
ensemblrs267607646
gopubmedrs267607646
geneviewrs267607646
scholarrs267607646
googlers267607646
pharmgkbrs267607646
gwascentralrs267607646
openSNPrs267607646
23andMers267607646
23andMe allrs267607646
SNP Nexus

SNPshotrs267607646
SNPdbers267607646
MSV3drs267607646
GWAS Ctlgrs267607646
Max Magnitude0
ClinVar
Risk rs267607646(G;G)
Alt rs267607646(G;G)
Reference rs267607646(;)
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.156085057dupG
CLNSRC ClinVar Epithelial Biology
CLNACC RCV000041344.2, RCV000057392.1,