Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267607555
rs267607555
LMNA
T 0.700 GeneticVariation CLINVAR Overlapping syndromes in laminopathies: a meta-analysis of the reported literature. 23853504

2013
dbSNP: rs267607555
rs267607555
LMNA
T 0.700 GeneticVariation CLINVAR Cosegregation of focal segmental glomerulosclerosis in a family with familial partial lipodystrophy due to a mutation in LMNA. 24080738

2013
dbSNP: rs267607555
rs267607555
LMNA
T 0.700 GeneticVariation CLINVAR Genotype-phenotype correlations in laminopathies: how does fate translate? 20074070

2010
dbSNP: rs267607555
rs267607555
LMNA
T 0.700 GeneticVariation CLINVAR Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations. 15219508

2004
dbSNP: rs267607555
rs267607555
LMNA
T 0.700 GeneticVariation CLINVAR Diagnostic validity of the MAST and the alcohol dependence scale in the assessment of DSM-III alcohol disorders. 2270059

1990