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.
Immune Reconstitution Inflammatory Syndrome
CUI: C1619738
Disease: Immune Reconstitution Inflammatory Syndrome
5 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2013 2013
Immune reconstitution syndrome
CUI: C1096197
Disease: Immune reconstitution syndrome
4 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2013 2013
Leprosy
CUI: C0023343
Disease: Leprosy
120 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2015 2015
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2018 2018
Lupus Nephritis
CUI: C0024143
Disease: Lupus Nephritis
64 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2018 2018
Malaria, Falciparum
CUI: C0024535
Disease: Malaria, Falciparum
19 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2007 2007
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2010 2010
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2018 2018
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2010 2010
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2018 2018
Microcephaly
CUI: C0025958
Disease: Microcephaly
27 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2019 2019
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2013 2013
Ocular Toxoplasmosis
CUI: C0040561
Disease: Ocular Toxoplasmosis
9 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2018 2018
Oropharyngeal disorders
CUI: C0553694
Disease: Oropharyngeal disorders
3 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2010 2010
Oropharynx (excludes nasopharynx)
CUI: C0549523
Disease: Oropharynx (excludes nasopharynx)
5 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2013 2013
Pain
CUI: C0030193
Disease: Pain
196 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2012 2012
Peptic Ulcer
CUI: C0030920
Disease: Peptic Ulcer
25 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2014 2014
Pouchitis
CUI: C0376620
Disease: Pouchitis
10 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2019 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2010 2010
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2020 2020
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2018 2018
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2018 2018