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rs267607578

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607578(A;A)
Make rs267607578(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position156136952
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607578
ebirs267607578
HLIrs267607578
Exacrs267607578
Varsomers267607578
Maprs267607578
PheGenIrs267607578
hapmaprs267607578
1000 genomesrs267607578
hgdprs267607578
ensemblrs267607578
gopubmedrs267607578
geneviewrs267607578
scholarrs267607578
googlers267607578
pharmgkbrs267607578
gwascentralrs267607578
openSNPrs267607578
23andMers267607578
23andMe allrs267607578
SNP Nexus

SNPshotrs267607578
SNPdbers267607578
MSV3drs267607578
GWAS Ctlgrs267607578
Max Magnitude0
ClinVar
Risk rs267607578(A;A)
Alt rs267607578(A;A)
Reference rs267607578(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy not provided Dilated cardiomyopathy 1A not specified
Variation info
Gene LMNA
CLNDBN Primary dilated cardiomyopathy not provided Dilated cardiomyopathy 1A not specified
Reversed 0
HGVS NC_000001.10:g.156106743G>A
CLNSRC Quest Diagnostics
CLNACC RCV000030148.3, RCV000057294.3, RCV000154177.3, RCV000235167.1,