MGLL, monoglyceride lipase, 11343

N. diseases: 125; N. variants: 7
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: rs17282209
rs17282209 		3 127996353 intron variant T/C snv 8.5E-02
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2015 2015
dbSNP: rs3773159
rs3773159 		1.000 0.080 3 127720095 intron variant C/T snv 0.16
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs6439106
rs6439106 		1.000 0.040 3 128000111 intron variant C/T snv 0.13
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.700 1.000 1 2019 2019
dbSNP: rs6439106
rs6439106 		1.000 0.040 3 128000111 intron variant C/T snv 0.13
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.700 1.000 1 2019 2019
dbSNP: rs664910
rs664910 		3 127755187 intron variant G/A snv 0.63
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.700 1.000 1 2013 2013
dbSNP: rs7634887
rs7634887 		3 127898762 intron variant C/A;G snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs9836225
rs9836225 		3 127797551 intron variant C/T snv 7.4E-03
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9836225
rs9836225 		3 127797551 intron variant C/T snv 7.4E-03
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9836225
rs9836225 		3 127797551 intron variant C/T snv 7.4E-03
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs604300
rs604300 		1.000 0.080 3 127724009 intron variant A/G snv 0.91
CUI: C0085281
Disease: Addictive Behavior
Addictive Behavior 		Behavior and Behavior Mechanisms 0.010 1.000 1 2015 2015
dbSNP: rs604300
rs604300 		1.000 0.080 3 127724009 intron variant A/G snv 0.91
CUI: C0013170
Disease: Drug habituation
Drug habituation 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs604300
rs604300 		1.000 0.080 3 127724009 intron variant A/G snv 0.91
CUI: C0006870
Disease: Cannabis Dependence
Cannabis Dependence 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2015 2015