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: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2006 2006
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2006 2006
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 1.000 1 2006 2006
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C0042345
Disease: Varicosity
Varicosity
0.010 1.000 1 2009 2009
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle
0.010 1.000 1 2010 2010
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C0158266
Disease: Intervertebral Disc Degeneration
Intervertebral Disc Degeneration
0.010 1.000 1 2013 2013
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C0017605
Disease: Angle Closure Glaucoma
Angle Closure Glaucoma
0.010 1.000 1 2013 2013
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C0149521
Disease: Pancreatitis, Chronic
Pancreatitis, Chronic
0.010 1.000 1 2013 2013
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis
0.010 < 0.001 1 2013 2013
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C0024031
Disease: Low Back Pain
Low Back Pain
0.010 1.000 1 2013 2013
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C0017606
Disease: Primary angle-closure glaucoma
Primary angle-closure glaucoma
0.010 1.000 1 2013 2013
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C0019270
Disease: Hernia
Hernia
0.010 1.000 1 2013 2013
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C0030193
Disease: Pain
Pain
0.010 1.000 1 2013 2013
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
0.020 1.000 2 2013 2014
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.020 1.000 2 2013 2014
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
Malignant neoplasm of urinary bladder
0.020 1.000 2 2013 2014
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
Aortic Aneurysm, Abdominal
0.010 1.000 1 2014 2014
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial
0.010 1.000 1 2015 2015
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 1.000 1 2015 2015
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary
0.010 1.000 1 2015 2015
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C0003165
Disease: Anthracosis
Anthracosis
0.010 1.000 1 2015 2015
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm
0.010 1.000 1 2015 2015
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C1568272
Disease: Tendinopathy
Tendinopathy
0.010 1.000 1 2016 2016
dbSNP: rs1799750
rs1799750
0.592 0.760 11 102799765 intron variant C/- delins 0.50
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.010 < 0.001 1 2016 2016