rs662, PON1

N. diseases: 157
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.
Congenital chromosomal disease
CUI: C0008626
Disease: Congenital chromosomal disease
47 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2019 2019
Exfoliation Syndrome
CUI: C0206368
Disease: Exfoliation Syndrome
74 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2019 2019
Glaucoma
CUI: C0017601
Disease: Glaucoma
198 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2019 2019
Hemorrhagic Fever, Crimean
CUI: C0019099
Disease: Hemorrhagic Fever, Crimean
9 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1 2019 2019
Hyperlipoproteinemia Type IIa
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
661 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2019 2019
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2019 2019
Osteoarthritis, Knee
CUI: C0409959
Disease: Osteoarthritis, Knee
150 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2019 2019
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2019 2019
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2019 2019
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.700 1.000 1 2018 2018
Diabetic macroangiopathy
CUI: C1504375
Disease: Diabetic macroangiopathy
2 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2018 2018
Disease of capillaries
CUI: C0155765
Disease: Disease of capillaries
5 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2018 2018
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1 2018 2018
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
197 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1 2018 2018
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.020 0.500 2 2017 2019
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1 2017 2017
Antiphospholipid Syndrome
CUI: C0085278
Disease: Antiphospholipid Syndrome
17 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2017 2017
Diabetes Mellitus, Insulin-Dependent
954 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2017 2017
Diabetic dyslipidaemia
CUI: C3160761
Disease: Diabetic dyslipidaemia
11 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1 2017 2017
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2017 2017
Polyendocrinopathies, Autoimmune
CUI: C0085409
Disease: Polyendocrinopathies, Autoimmune
21 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1 2017 2017
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2016 2016
Hyperhomocysteinemia
CUI: C0598608
Disease: Hyperhomocysteinemia
45 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2016 2016
Lupus anticoagulant disorder
CUI: C0311370
Disease: Lupus anticoagulant disorder
14 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2016 2016
ST segment elevation myocardial infarction
16 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2016 2016