FBN2, fibrillin 2, 2201

N. diseases: 211; N. variants: 42
Disease: Marfan Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519321
rs1057519321
Entrez Id: 2201
Gene Symbol: FBN2
FBN2
CUI: C0024796
Disease:
Marfan Syndrome 		A 0.700 GeneticVariation CLINVAR