Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0030193
Disease: Pain
Pain
0.010 1.000 1 2012 2012
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.010 1.000 1 2018 2018
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0549523
Disease: Oropharynx (excludes nasopharynx)
Oropharynx (excludes nasopharynx)
0.010 1.000 1 2013 2013
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2010 2010
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0040561
Disease: Ocular Toxoplasmosis
Ocular Toxoplasmosis
0.010 1.000 1 2018 2018
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C4552332
Disease: Congenital Zika syndrome
Congenital Zika syndrome
0.010 1.000 1 2019 2019
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C2747816
Disease: Complicated malaria
Complicated malaria
0.010 1.000 1 2007 2007
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0206081
Disease: Hyperandrogenism
Hyperandrogenism
0.010 1.000 1 2013 2013
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.010 1.000 1 2016 2016
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0030920
Disease: Peptic Ulcer
Peptic Ulcer
0.010 1.000 1 2014 2014
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome
0.010 1.000 1 2016 2016
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.010 1.000 1 2015 2015
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0376620
Disease: Pouchitis
Pouchitis
0.010 1.000 1 2019 2019
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0023343
Disease: Leprosy
Leprosy
0.010 1.000 1 2015 2015
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis
0.010 1.000 1 2016 2016
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2013 2013
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.010 1.000 1 2016 2016
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0025958
Disease: Microcephaly
Microcephaly
0.010 1.000 1 2019 2019
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0008707
Disease: Chronic osteomyelitis
Chronic osteomyelitis
0.010 1.000 1 2018 2018
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2010 2010
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2010 2010
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.010 1.000 1 2016 2016
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.010 1.000 1 2020 2020