Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555405044
rs1555405044
G 0.700 CausalMutation CLINVAR Increased frequency of FBN1 truncating and splicing variants in Marfan syndrome patients with aortic events. 25101912

2015

dbSNP: rs1555405044
rs1555405044
G 0.700 CausalMutation CLINVAR Dural ectasia and FBN1 mutation screening of 40 patients with Marfan syndrome and related disorders: role of dural ectasia for the diagnosis. 23684891

2013

dbSNP: rs1555405044
rs1555405044
G 0.700 CausalMutation CLINVAR Effect of mutation type and location on clinical outcome in 1,013 probands with Marfan syndrome or related phenotypes and FBN1 mutations: an international study. 17701892

2007

dbSNP: rs1555405044
rs1555405044
G 0.700 CausalMutation CLINVAR Application of dHPLC for mutation detection of the fibrillin-1 gene for the diagnosis of Marfan syndrome in a National Health Service Laboratory. 17627385

2007

dbSNP: rs1555405044
rs1555405044
G 0.700 CausalMutation CLINVAR Fibrillin-1 misfolding and disease. 16677079

2006

dbSNP: rs1555405044
rs1555405044
G 0.700 CausalMutation CLINVAR The molecular genetics of Marfan syndrome and related disorders. 16571647

2006

dbSNP: rs1555405044
rs1555405044
G 0.700 CausalMutation CLINVAR Cysteine substitutions in epidermal growth factor-like domains of fibrillin-1: distinct effects on biochemical and clinical phenotypes. 10486319

1999

dbSNP: rs1555405044
rs1555405044
G 0.700 CausalMutation CLINVAR The solution structure of human epidermal growth factor. 3495735

1987

dbSNP: rs1555405044
rs1555405044
G 0.700 CausalMutation CLINVAR Epidermal growth factor. Location of disulfide bonds. 4750422

1973