Source: BEFREE

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: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.060 1.000 6 2009 2013
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0017606
Disease: Primary angle-closure glaucoma
Primary angle-closure glaucoma
0.050 0.800 5 2009 2020
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0017605
Disease: Angle Closure Glaucoma
Angle Closure Glaucoma
0.050 0.800 5 2009 2020
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0004096
Disease: Asthma
Asthma
0.030 0.333 3 2005 2019
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.030 0.667 3 2009 2013
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.020 1.000 2 2016 2017
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0022578
Disease: Keratoconus
Keratoconus
0.020 1.000 2 2017 2020
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.020 1.000 2 2015 2017
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0158266
Disease: Intervertebral Disc Degeneration
Intervertebral Disc Degeneration
0.020 1.000 2 2017 2018
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle
0.020 1.000 2 2010 2013
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.020 1.000 2 2005 2010
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.020 0.500 2 2012 2018
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0014175
Disease: Endometriosis
Endometriosis
0.020 0.500 2 2009 2016
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0281899
Disease: Prolapsed lumbar disc
Prolapsed lumbar disc
0.020 1.000 2 2008 2018
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 0.500 2 2010 2018
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.020 0.500 2 2010 2018
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0392525
Disease: Nephrolithiasis
Nephrolithiasis
0.010 1.000 1 2018 2018
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.010 1.000 1 2011 2011
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.010 1.000 1 2009 2009
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C2931384
Disease: Moyamoya disease 1
Moyamoya disease 1
0.010 1.000 1 2014 2014
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0278595
Disease: Adult Fibrosarcoma
Adult Fibrosarcoma
0.010 1.000 1 1994 1994
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 1.000 1 2012 2012
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
Malignant neoplasm of urinary bladder
0.010 1.000 1 2010 2010
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
Conventional (Clear Cell) Renal Cell Carcinoma
0.010 1.000 1 2006 2006
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0025289
Disease: Meningitis
Meningitis
0.010 1.000 1 2018 2018