ALOX15, arachidonate 15-lipoxygenase, 246

N. diseases: 205; N. variants: 5
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs34210653
rs34210653 		0.807 0.280 17 4632019 missense variant G/A snv 2.7E-02 1.7E-02
CUI: C0027430
Disease: Nasal Polyps
Nasal Polyps 		Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases 0.710 1.000 1 2019 2019
dbSNP: rs113604586
rs113604586 		17 4639054 missense variant T/C snv 1.7E-03 1.6E-03
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs113604586
rs113604586 		17 4639054 missense variant T/C snv 1.7E-03 1.6E-03
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs34210653
rs34210653 		0.807 0.280 17 4632019 missense variant G/A snv 2.7E-02 1.7E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs34210653
rs34210653 		0.807 0.280 17 4632019 missense variant G/A snv 2.7E-02 1.7E-02
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs34210653
rs34210653 		0.807 0.280 17 4632019 missense variant G/A snv 2.7E-02 1.7E-02
CUI: C0149516
Disease: Chronic sinusitis
Chronic sinusitis 		Infections; Respiratory Tract Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2019 2019
dbSNP: rs34210653
rs34210653 		0.807 0.280 17 4632019 missense variant G/A snv 2.7E-02 1.7E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.030 1.000 3 2008 2011
dbSNP: rs2619112
rs2619112 		0.882 0.160 17 4632090 intron variant A/C;G snv 4.0E-06; 0.53
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.020 1.000 2 2010 2018
dbSNP: rs7217186
rs7217186 		0.827 0.120 17 4636097 intron variant C/T snv 0.45
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.020 1.000 2 2010 2018
dbSNP: rs11568070
rs11568070 		1.000 0.040 17 4641943 intron variant G/A snv 2.0E-02
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2619112
rs2619112 		0.882 0.160 17 4632090 intron variant A/C;G snv 4.0E-06; 0.53
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs2619112
rs2619112 		0.882 0.160 17 4632090 intron variant A/C;G snv 4.0E-06; 0.53
CUI: C0007113
Disease: Rectal Carcinoma
Rectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs34210653
rs34210653 		0.807 0.280 17 4632019 missense variant G/A snv 2.7E-02 1.7E-02
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.010 1.000 1 2019 2019
dbSNP: rs34210653
rs34210653 		0.807 0.280 17 4632019 missense variant G/A snv 2.7E-02 1.7E-02
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs34210653
rs34210653 		0.807 0.280 17 4632019 missense variant G/A snv 2.7E-02 1.7E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs7217186
rs7217186 		0.827 0.120 17 4636097 intron variant C/T snv 0.45
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs7217186
rs7217186 		0.827 0.120 17 4636097 intron variant C/T snv 0.45
CUI: C3714731
Disease: Early childhood caries
Early childhood caries 		Stomatognathic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs7217186
rs7217186 		0.827 0.120 17 4636097 intron variant C/T snv 0.45
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs7217186
rs7217186 		0.827 0.120 17 4636097 intron variant C/T snv 0.45
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2012 2012