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

rs267607594

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607594(C;C)
Make rs267607594(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position156130745
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607594
ebirs267607594
HLIrs267607594
Exacrs267607594
Varsomers267607594
Maprs267607594
PheGenIrs267607594
hapmaprs267607594
1000 genomesrs267607594
hgdprs267607594
ensemblrs267607594
gopubmedrs267607594
geneviewrs267607594
scholarrs267607594
googlers267607594
pharmgkbrs267607594
gwascentralrs267607594
openSNPrs267607594
23andMers267607594
23andMe allrs267607594
SNP Nexus

SNPshotrs267607594
SNPdbers267607594
MSV3drs267607594
GWAS Ctlgrs267607594
Max Magnitude0
ClinVar
Risk rs267607594(C;C)
Alt rs267607594(C;C)
Reference rs267607594(T;T)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy not provided
Variation info
Gene LMNA
CLNDBN Primary dilated cardiomyopathy not provided
Reversed 0
HGVS NC_000001.10:g.156100536T>C
CLNSRC ClinVar Epithelial Biology
CLNACC RCV000041352.2, RCV000057410.1,