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rs267607554

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607554(C;T)
Make rs267607554(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position156135925
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607554
ebirs267607554
HLIrs267607554
Exacrs267607554
Varsomers267607554
Maprs267607554
PheGenIrs267607554
hapmaprs267607554
1000 genomesrs267607554
hgdprs267607554
ensemblrs267607554
gopubmedrs267607554
geneviewrs267607554
scholarrs267607554
googlers267607554
pharmgkbrs267607554
gwascentralrs267607554
openSNPrs267607554
23andMers267607554
23andMe allrs267607554
SNP Nexus

SNPshotrs267607554
SNPdbers267607554
MSV3drs267607554
GWAS Ctlgrs267607554
Max Magnitude0
ClinVar
Risk rs267607554(T;T)
Alt rs267607554(T;T)
Reference rs267607554(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.156105716C>T
CLNSRC ClinVar Epithelial Biology
CLNACC RCV000041382.3, RCV000057493.3,