rs6568431, ATG5

N. diseases: 7
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.
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.790 0.320 6 106140931 intron variant A/C snv 0.61 0.800 1.000 5 2008 2017
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.790 0.320 6 106140931 intron variant A/C snv 0.61 0.700 1.000 1 2011 2011
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.790 0.320 6 106140931 intron variant A/C snv 0.61 0.700 1.000 1 2017 2017
Anemia
CUI: C0002871
Disease: Anemia
94 0.790 0.320 6 106140931 intron variant A/C snv 0.61 0.010 1.000 1 2018 2018
Cerebral Palsy
CUI: C0007789
Disease: Cerebral Palsy
69 0.790 0.320 6 106140931 intron variant A/C snv 0.61 0.010 1.000 1 2017 2017
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.790 0.320 6 106140931 intron variant A/C snv 0.61 0.010 1.000 1 2019 2019
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.790 0.320 6 106140931 intron variant A/C snv 0.61 0.010 1.000 1 2019 2019