FBN2, fibrillin 2, 2201

N. diseases: 211; N. variants: 42
Disease: MACULAR DEGENERATION, EARLY-ONSET ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs200060005
rs200060005
Entrez Id: 2201
Gene Symbol: FBN2
FBN2
CUI: C4015286
Disease:
MACULAR DEGENERATION, EARLY-ONSET 		0.700 GeneticVariation UNIPROT Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration. 24899048 2014
dbSNP: rs149054177
rs149054177
Entrez Id: 2201
Gene Symbol: FBN2
FBN2
CUI: C4015286
Disease:
MACULAR DEGENERATION, EARLY-ONSET 		0.700 GeneticVariation UNIPROT