Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555399271
rs1555399271
T 0.700 CausalMutation CLINVAR A novel FBN1 heterozygous mutation identified in a Chinese family with autosomal dominant Marfan syndrome. 25966184

2015

dbSNP: rs1555399271
rs1555399271
T 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: rs1555399271
rs1555399271
T 0.700 CausalMutation CLINVAR Fibrillin-1 misfolding and disease. 16677079

2006

dbSNP: rs1555399271
rs1555399271
T 0.700 CausalMutation CLINVAR The molecular genetics of Marfan syndrome and related disorders. 16571647

2006

dbSNP: rs1555399271
rs1555399271
T 0.700 CausalMutation CLINVAR Identification of 29 novel and nine recurrent fibrillin-1 (FBN1) mutations and genotype-phenotype correlations in 76 patients with Marfan syndrome. 16220557

2005

dbSNP: rs1555399271
rs1555399271
T 0.700 CausalMutation CLINVAR Genotype and phenotype analysis of 171 patients referred for molecular study of the fibrillin-1 gene FBN1 because of suspected Marfan syndrome. 11700157

2001

dbSNP: rs1555399271
rs1555399271
T 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: rs1555399271
rs1555399271
T 0.700 CausalMutation CLINVAR The solution structure of human epidermal growth factor. 3495735

1987

dbSNP: rs1555399271
rs1555399271
T 0.700 CausalMutation CLINVAR Epidermal growth factor. Location of disulfide bonds. 4750422

1973