rs121909715, GSN

N. diseases: 8
Disease: Corneal dystrophy, Lattice type 3 ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Corneal dystrophy, Lattice type 3
CUI: C0339273
Disease: Corneal dystrophy, Lattice type 3
0.010 GeneticVariation BEFREE A patient having Finnish-type corneal amyloidosis had a p.D187N mutation in GSN. 24801599 2014