rs10818488, C5-OT1

N. diseases: 8
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.
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.776 0.360 9 120942809 regulatory region variant A/G snv 0.51 0.090 1.000 9 2008 2014
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.776 0.360 9 120942809 regulatory region variant A/G snv 0.51 0.050 1.000 5 2008 2013
Acquired aplastic anemia
CUI: C0271907
Disease: Acquired aplastic anemia
12 0.776 0.360 9 120942809 regulatory region variant A/G snv 0.51 0.010 1 2015 2015
Aplastic Anemia
CUI: C0002874
Disease: Aplastic Anemia
30 0.776 0.360 9 120942809 regulatory region variant A/G snv 0.51 0.010 1 2015 2015
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.776 0.360 9 120942809 regulatory region variant A/G snv 0.51 0.010 1.000 1 2019 2019
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.776 0.360 9 120942809 regulatory region variant A/G snv 0.51 0.010 1.000 1 2010 2010
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.776 0.360 9 120942809 regulatory region variant A/G snv 0.51 0.010 1.000 1 2016 2016
Neurocysticercosis
CUI: C0338437
Disease: Neurocysticercosis
9 0.776 0.360 9 120942809 regulatory region variant A/G snv 0.51 0.010 1.000 1 2019 2019