PXDN, peroxidasin, 7837

N. diseases: 51; N. variants: 8
Disease: Anterior segment mesenchymal dysgenesis ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1558489563
rs1558489563 		1.000 0.080 2 1649321 missense variant T/C snv
CUI: C1862839
Disease: Anterior segment mesenchymal dysgenesis
Anterior segment mesenchymal dysgenesis 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.700 0