Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs113393517
rs113393517
FBN1
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome 		G 0.710 GeneticVariation CLINVAR

dbSNP: rs113393517
rs113393517
FBN1
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome 		A 0.710 GeneticVariation CLINVAR