MIP, major intrinsic protein of lens fiber, 4284

N. diseases: 181; N. variants: 21
Disease: Congenital lamellar cataract ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121917869
rs121917869
Entrez Id: 4284
Gene Symbol: MIP
MIP
CUI: C0266537
Disease:
Congenital lamellar cataract 		0.010 GeneticVariation BEFREE Families with E134G have a uni-lamellar cataract which is stable after birth, whereas families with T138R have multi-focal opacities which increase throughout life. 11001937 2000