ATG5, autophagy related 5, 9474

N. diseases: 282; N. variants: 36
Disease: Anemia ×
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: rs2245214
rs2245214 		0.827 0.240 6 106214866 intron variant C/G snv 0.42
CUI: C0002871
Disease: Anemia
Anemia 		Hemic and Lymphatic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs6568431
rs6568431 		0.790 0.320 6 106140931 intron variant A/C snv 0.61
CUI: C0002871
Disease: Anemia
Anemia 		Hemic and Lymphatic Diseases 0.010 1.000 1 2018 2018