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rs267607573

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607573(C;T)
Make rs267607573(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position156134865
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607573
ebirs267607573
HLIrs267607573
Exacrs267607573
Varsomers267607573
Maprs267607573
PheGenIrs267607573
hapmaprs267607573
1000 genomesrs267607573
hgdprs267607573
ensemblrs267607573
gopubmedrs267607573
geneviewrs267607573
scholarrs267607573
googlers267607573
pharmgkbrs267607573
gwascentralrs267607573
openSNPrs267607573
23andMers267607573
23andMe allrs267607573
SNP Nexus

SNPshotrs267607573
SNPdbers267607573
MSV3drs267607573
GWAS Ctlgrs267607573
Max Magnitude0
ClinVar
Risk rs267607573(T;T)
Alt rs267607573(T;T)
Reference rs267607573(C;C)
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.156104656C>T
CLNSRC ClinVar Epithelial Biology
CLNACC RCV000041360.2, RCV000057446.1,