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rs267607593

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607593(C;C)
Make rs267607593(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position156134964
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607593
ebirs267607593
HLIrs267607593
Exacrs267607593
Varsomers267607593
Maprs267607593
PheGenIrs267607593
hapmaprs267607593
1000 genomesrs267607593
hgdprs267607593
ensemblrs267607593
gopubmedrs267607593
geneviewrs267607593
scholarrs267607593
googlers267607593
pharmgkbrs267607593
gwascentralrs267607593
openSNPrs267607593
23andMers267607593
23andMe allrs267607593
SNP Nexus

SNPshotrs267607593
SNPdbers267607593
MSV3drs267607593
GWAS Ctlgrs267607593
Max Magnitude0
ClinVar
Risk rs267607593(C;C)
Alt rs267607593(C;C)
Reference rs267607593(T;T)
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.156104755T>C
CLNSRC ClinVar Epithelial Biology
CLNACC RCV000041369.2, RCV000057461.3,