Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267607637
rs267607637
LMNA
A 0.700 CausalMutation CLINVAR Myopathic lamin mutations cause reductive stress and activate the nrf2/keap-1 pathway. 25996830

2015
dbSNP: rs267607637
rs267607637
LMNA
A 0.700 CausalMutation CLINVAR Mapping disease-related missense mutations in the immunoglobulin-like fold domain of lamin A/C reveals novel genotype-phenotype associations for laminopathies. 24375749

2014