CNR2, cannabinoid receptor 2, 1269

N. diseases: 197; 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: rs2501426
rs2501426 		1 23872874 3 prime UTR variant G/A snv 0.63
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs2502994
rs2502994 		1 23872873 3 prime UTR variant T/A;C snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs2502994
rs2502994 		1 23872873 3 prime UTR variant T/A;C snv
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs2501431
rs2501431 		1.000 0.080 1 23875153 synonymous variant G/A snv 0.62 0.64
CUI: C0029456
Disease: Osteoporosis
Osteoporosis 		Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.020 1.000 2 2015 2019
dbSNP: rs2501432
rs2501432 		0.716 0.480 1 23875430 missense variant T/C;G snv 0.62
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.020 1.000 2 2010 2013
dbSNP: rs2501432
rs2501432 		0.716 0.480 1 23875430 missense variant T/C;G snv 0.62
CUI: C0398650
Disease: Immune thrombocytopenic purpura
Immune thrombocytopenic purpura 		Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases 0.020 1.000 2 2011 2013
dbSNP: rs2501432
rs2501432 		0.716 0.480 1 23875430 missense variant T/C;G snv 0.62
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.020 0.500 2 2014 2019
dbSNP: rs2501432
rs2501432 		0.716 0.480 1 23875430 missense variant T/C;G snv 0.62
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		Digestive System Diseases; Nutritional and Metabolic Diseases 0.020 1.000 2 2012 2018
dbSNP: rs3003336
rs3003336 		1.000 0.080 1 23874958 synonymous variant C/T snv 0.62 0.64
CUI: C0029456
Disease: Osteoporosis
Osteoporosis 		Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.020 1.000 2 2015 2019
dbSNP: rs35761398
rs35761398 		0.701 0.520 1 23875429 missense variant TT/CC mnv
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		Digestive System Diseases; Nutritional and Metabolic Diseases 0.020 1.000 2 2012 2018
dbSNP: rs35761398
rs35761398 		0.701 0.520 1 23875429 missense variant TT/CC mnv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.020 0.500 2 2014 2019
dbSNP: rs35761398
rs35761398 		0.701 0.520 1 23875429 missense variant TT/CC mnv
CUI: C0398650
Disease: Immune thrombocytopenic purpura
Immune thrombocytopenic purpura 		Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases 0.020 1.000 2 2011 2013
dbSNP: rs879761216
rs879761216 		0.732 0.480 1 23875429 frameshift variant TT/C;T delins
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.020 0.500 2 2014 2019
dbSNP: rs879761216
rs879761216 		0.732 0.480 1 23875429 frameshift variant TT/C;T delins
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		Digestive System Diseases; Nutritional and Metabolic Diseases 0.020 1.000 2 2012 2018
dbSNP: rs879761216
rs879761216 		0.732 0.480 1 23875429 frameshift variant TT/C;T delins
CUI: C0398650
Disease: Immune thrombocytopenic purpura
Immune thrombocytopenic purpura 		Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases 0.020 1.000 2 2011 2013
dbSNP: rs2229579
rs2229579 		0.925 0.120 1 23874672 missense variant G/A;T snv 0.10; 8.0E-06
CUI: C0029456
Disease: Osteoporosis
Osteoporosis 		Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.010 < 0.001 1 2019 2019
dbSNP: rs2229579
rs2229579 		0.925 0.120 1 23874672 missense variant G/A;T snv 0.10; 8.0E-06
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs2501401
rs2501401 		1.000 0.040 1 23893573 intron variant A/C;G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs2501432
rs2501432 		0.716 0.480 1 23875430 missense variant T/C;G snv 0.62
CUI: C0003864
Disease: Arthritis
Arthritis 		Musculoskeletal Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2501432
rs2501432 		0.716 0.480 1 23875430 missense variant T/C;G snv 0.62
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2501432
rs2501432 		0.716 0.480 1 23875430 missense variant T/C;G snv 0.62
CUI: C1442786
Disease: Acute respiratory tract infection
Acute respiratory tract infection 		Infections; Respiratory Tract Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2501432
rs2501432 		0.716 0.480 1 23875430 missense variant T/C;G snv 0.62
CUI: C0013473
Disease: Eating Disorders
Eating Disorders 		Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs2501432
rs2501432 		0.716 0.480 1 23875430 missense variant T/C;G snv 0.62
CUI: C0029456
Disease: Osteoporosis
Osteoporosis 		Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2501432
rs2501432 		0.716 0.480 1 23875430 missense variant T/C;G snv 0.62
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2020 2020
dbSNP: rs2501432
rs2501432 		0.716 0.480 1 23875430 missense variant T/C;G snv 0.62
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2007 2007