C9, complement C9, 735

N. diseases: 62; N. variants: 32
Disease: Geographic Atrophy ×
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: rs62358361
rs62358361 		0.851 0.040 5 39327786 intron variant G/C;T snv
CUI: C1536085
Disease: Geographic Atrophy
Geographic Atrophy 		Eye Diseases 0.700 1.000 1 2016 2016