AHR, aryl hydrocarbon receptor, 196

N. diseases: 532; N. variants: 20
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: rs2158041
rs2158041 		0.807 0.160 7 17328796 intron variant T/C snv 0.81
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2158041
rs2158041 		0.807 0.160 7 17328796 intron variant T/C snv 0.81
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2158041
rs2158041 		0.807 0.160 7 17328796 intron variant T/C snv 0.81
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2009 2009
dbSNP: rs2158041
rs2158041 		0.807 0.160 7 17328796 intron variant T/C snv 0.81
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2009 2009
dbSNP: rs2158041
rs2158041 		0.807 0.160 7 17328796 intron variant T/C snv 0.81
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2009 2009
dbSNP: rs2158041
rs2158041 		0.807 0.160 7 17328796 intron variant T/C snv 0.81
CUI: C0017638
Disease: Glioma
Glioma 		Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs7796976
rs7796976 		0.925 0.040 7 17298806 5 prime UTR variant A/G snv 0.79
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs7796976
rs7796976 		0.925 0.040 7 17298806 5 prime UTR variant A/G snv 0.79
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs7796976
rs7796976 		0.925 0.040 7 17298806 5 prime UTR variant A/G snv 0.79
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs7811989
rs7811989 		0.882 0.080 7 17331739 intron variant A/G snv 0.76
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.020 1.000 2 2009 2018
dbSNP: rs7811989
rs7811989 		0.882 0.080 7 17331739 intron variant A/G snv 0.76
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.020 1.000 2 2009 2018
dbSNP: rs7811989
rs7811989 		0.882 0.080 7 17331739 intron variant A/G snv 0.76
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.020 1.000 2 2009 2018
dbSNP: rs4410790
rs4410790 		0.882 0.160 7 17244953 intron variant T/C snv 0.54
CUI: C0236734
Disease: Caffeine related disorders
Caffeine related disorders 		0.030 1.000 3 2012 2017
dbSNP: rs4410790
rs4410790 		0.882 0.160 7 17244953 intron variant T/C snv 0.54
CUI: C0202194
Disease: Potassium measurement
Potassium measurement 		0.700 1.000 1 2019 2019
dbSNP: rs4410790
rs4410790 		0.882 0.160 7 17244953 intron variant T/C snv 0.54
CUI: C0001925
Disease: Albuminuria
Albuminuria 		Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2018 2018
dbSNP: rs4410790
rs4410790 		0.882 0.160 7 17244953 intron variant T/C snv 0.54
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs4410790
rs4410790 		0.882 0.160 7 17244953 intron variant T/C snv 0.54
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs4410790
rs4410790 		0.882 0.160 7 17244953 intron variant T/C snv 0.54
CUI: C0337443
Disease: Sodium measurement
Sodium measurement 		0.700 1.000 1 2019 2019
dbSNP: rs4410790
rs4410790 		0.882 0.160 7 17244953 intron variant T/C snv 0.54
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.010 < 0.001 1 2017 2017
dbSNP: rs4410790
rs4410790 		0.882 0.160 7 17244953 intron variant T/C snv 0.54
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.010 < 0.001 1 2017 2017
dbSNP: rs4410790
rs4410790 		0.882 0.160 7 17244953 intron variant T/C snv 0.54
CUI: C0730345
Disease: Microalbuminuria
Microalbuminuria 		Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2019 2019
dbSNP: rs6968865
rs6968865 		7 17247645 5 prime UTR variant A/T snv 0.54
CUI: C0236734
Disease: Caffeine related disorders
Caffeine related disorders 		0.020 1.000 2 2012 2016
dbSNP: rs1525735
rs1525735 		0.827 0.120 7 17157947 intron variant C/T snv 0.49
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs1525735
rs1525735 		0.827 0.120 7 17157947 intron variant C/T snv 0.49
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		Musculoskeletal Diseases 0.700 1.000 1 2016 2016
dbSNP: rs1525735
rs1525735 		0.827 0.120 7 17157947 intron variant C/T snv 0.49
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2016 2016