LTA4H, leukotriene A4 hydrolase, 4048

N. diseases: 63; N. variants: 11
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: rs2072510
rs2072510 		12 96009421 non coding transcript exon variant G/A snv 0.49
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2016 2016
dbSNP: rs2072510
rs2072510 		12 96009421 non coding transcript exon variant G/A snv 0.49
CUI: C0201874
Disease: Amino acids measurement
Amino acids measurement 		0.700 1.000 1 2016 2016
dbSNP: rs2540500
rs2540500 		12 96005050 intron variant T/C snv 0.84
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs17525488
rs17525488 		1.000 0.080 12 96035660 intron variant T/- delins
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs17525495
rs17525495 		0.882 0.080 12 96035599 5 prime UTR variant G/A snv 9.9E-02
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		Infections 0.010 1.000 1 2016 2016
dbSNP: rs17525495
rs17525495 		0.882 0.080 12 96035599 5 prime UTR variant G/A snv 9.9E-02
CUI: C0085437
Disease: Meningitis, Bacterial
Meningitis, Bacterial 		Infections; Nervous System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs17525495
rs17525495 		0.882 0.080 12 96035599 5 prime UTR variant G/A snv 9.9E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs17525495
rs17525495 		0.882 0.080 12 96035599 5 prime UTR variant G/A snv 9.9E-02
CUI: C0275911
Disease: Tuberculosis of intestines
Tuberculosis of intestines 		Digestive System Diseases; Infections 0.010 < 0.001 1 2019 2019
dbSNP: rs1978331
rs1978331 		0.827 0.200 12 96015423 intron variant A/G snv 0.50
CUI: C0679362
Disease: Tuberculosis, extrapulmonary
Tuberculosis, extrapulmonary 		Infections 0.010 1.000 1 2014 2014
dbSNP: rs1978331
rs1978331 		0.827 0.200 12 96015423 intron variant A/G snv 0.50
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1978331
rs1978331 		0.827 0.200 12 96015423 intron variant A/G snv 0.50
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs1978331
rs1978331 		0.827 0.200 12 96015423 intron variant A/G snv 0.50
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1978331
rs1978331 		0.827 0.200 12 96015423 intron variant A/G snv 0.50
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary 		Infections; Respiratory Tract Diseases 0.010 1.000 1 2011 2011
dbSNP: rs2247570
rs2247570 		1.000 0.080 12 96028599 intron variant T/C snv 0.33
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs2540477
rs2540477 		1.000 0.040 12 96043776 upstream gene variant G/A snv 0.77
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs2540487
rs2540487 		1.000 0.080 12 96036005 intron variant C/A;G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2540493
rs2540493 		1.000 0.080 12 96022064 intron variant A/C snv 0.17
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs2660898
rs2660898 		1.000 0.080 12 96032219 intron variant T/G snv 0.30
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary 		Infections; Respiratory Tract Diseases 0.010 1.000 1 2011 2011
dbSNP: rs6538697
rs6538697 		1.000 0.080 12 96009832 non coding transcript exon variant T/C snv 0.13
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs6538697
rs6538697 		1.000 0.080 12 96009832 non coding transcript exon variant T/C snv 0.13
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2012 2012