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 0.752 0.400 8 118952831 upstream gene variant T/C snv 0.17 0.040 0.250 4 2014 2019
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
182 0.752 0.400 8 118952831 upstream gene variant T/C snv 0.17 0.020 1.000 2 2014 2019
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.752 0.400 8 118952831 upstream gene variant T/C snv 0.17 0.010 1.000 1 2013 2013
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.752 0.400 8 118952831 upstream gene variant T/C snv 0.17 0.010 1.000 1 2017 2017
Hyperparathyroidism, Primary
CUI: C0221002
Disease: Hyperparathyroidism, Primary
39 0.752 0.400 8 118952831 upstream gene variant T/C snv 0.17 0.010 1 2011 2011
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.752 0.400 8 118952831 upstream gene variant T/C snv 0.17 0.010 1.000 1 2017 2017
Large-artery atherosclerosis (embolus/thrombosis)
CUI: C4699512
Disease: Large-artery atherosclerosis (embolus/thrombosis)
35 0.752 0.400 8 118952831 upstream gene variant T/C snv 0.17 0.010 1.000 1 2017 2017
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.752 0.400 8 118952831 upstream gene variant T/C snv 0.17 0.010 1.000 1 2013 2013
Osteoporotic Fractures
CUI: C0521170
Disease: Osteoporotic Fractures
40 0.752 0.400 8 118952831 upstream gene variant T/C snv 0.17 0.010 1.000 1 2017 2017
Periodontitis
CUI: C0031099
Disease: Periodontitis
116 0.752 0.400 8 118952831 upstream gene variant T/C snv 0.17 0.010 1.000 1 2019 2019
Root Resorption
CUI: C0035851
Disease: Root Resorption
7 0.752 0.400 8 118952831 upstream gene variant T/C snv 0.17 0.010 1.000 1 2014 2014
Vascular stenosis
CUI: C0679403
Disease: Vascular stenosis
3 0.752 0.400 8 118952831 upstream gene variant T/C snv 0.17 0.010 1.000 1 2017 2017