Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs140592
rs140592
FBN1
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome 		G 0.800 GeneticVariation CLINVAR FBN1: The disease-causing gene for Marfan syndrome and other genetic disorders. 27437668

2016
dbSNP: rs140592
rs140592
FBN1
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome 		G 0.800 GeneticVariation 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: rs140592
rs140592
FBN1
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome 		G 0.800 GeneticVariation CLINVAR The molecular genetics of Marfan syndrome and related disorders. 16571647

2006
dbSNP: rs140592
rs140592
FBN1
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome 		G 0.800 GeneticVariation CLINVAR Specific sequence motif of 8-Cys repeats of TGF-beta binding proteins, LTBPs, creates a hydrophobic interaction surface for binding of small latent TGF-beta. 10930463

2000
dbSNP: rs140592
rs140592
FBN1
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome 		G 0.800 GeneticVariation CLINVAR Marfan Database (third edition): new mutations and new routines for the software. 9399842

1998