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: rs35761398
rs35761398 		0.701 0.520 1 23875429 missense variant TT/CC mnv
CUI: C1698259
Disease: HCV coinfection
HCV coinfection 		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: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2007 2007
dbSNP: rs35761398
rs35761398 		0.701 0.520 1 23875429 missense variant TT/CC mnv
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2007 2007
dbSNP: rs879761216
rs879761216 		0.732 0.480 1 23875429 frameshift variant TT/C;T delins
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2007 2007
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: 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: 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: 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: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs35761398
rs35761398 		0.701 0.520 1 23875429 missense variant TT/CC mnv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs35761398
rs35761398 		0.701 0.520 1 23875429 missense variant TT/CC mnv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs879761216
rs879761216 		0.732 0.480 1 23875429 frameshift variant TT/C;T delins
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs879761216
rs879761216 		0.732 0.480 1 23875429 frameshift variant TT/C;T delins
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs35761398
rs35761398 		0.701 0.520 1 23875429 missense variant TT/CC mnv
CUI: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic 		Digestive System Diseases; Infections 0.010 1.000 1 2015 2015
dbSNP: rs35761398
rs35761398 		0.701 0.520 1 23875429 missense variant TT/CC mnv
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.010 1.000 1 2014 2014
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: 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: 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: 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: rs35761398
rs35761398 		0.701 0.520 1 23875429 missense variant TT/CC mnv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2020 2020
dbSNP: rs879761216
rs879761216 		0.732 0.480 1 23875429 frameshift variant TT/C;T delins
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2020 2020
dbSNP: rs35761398
rs35761398 		0.701 0.520 1 23875429 missense variant TT/CC mnv
CUI: C0019693
Disease: HIV Infections
HIV Infections 		Infections; Immune System Diseases 0.010 1.000 1 2018 2018