rs387907339, CRYAB

N. diseases: 4
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Alpha-B Crystallinopathy
CUI: C1837317
Disease: Alpha-B Crystallinopathy
4 0.882 0.280 11 111908967 missense variant C/A;G snv 0.700 0
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.882 0.280 11 111908967 missense variant C/A;G snv 0.010 1.000 1 2012 2012
Cataract
CUI: C0086543
Disease: Cataract
124 0.882 0.280 11 111908967 missense variant C/A;G snv 0.010 1.000 1 2020 2020
Congenital cataract
CUI: C0009691
Disease: Congenital cataract
104 0.882 0.280 11 111908967 missense variant C/A;G snv 0.010 1.000 1 2020 2020