DPP4, dipeptidyl peptidase 4, 1803

N. diseases: 451; N. variants: 13
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: rs12617656
rs12617656 		0.925 0.200 2 161994637 intron variant T/C snv 0.35
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.800 1.000 1 2014 2014
dbSNP: rs2268894
rs2268894 		2 161999638 intron variant C/T snv 0.56
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 2 2017 2018
dbSNP: rs2284871
rs2284871 		2 162031545 intron variant C/T snv 0.32
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 2 2018 2018
dbSNP: rs6741949
rs6741949 		2 162053713 intron variant G/C snv 0.33
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 2 2018 2019
dbSNP: rs12621633
rs12621633 		2 162002926 intron variant G/A snv 1.0E-02
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs145965241
rs145965241 		2 162011117 intron variant A/G snv 7.0E-03
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2268894
rs2268894 		2 161999638 intron variant C/T snv 0.56
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs2389643
rs2389643 		2 162010482 intron variant C/T snv 9.2E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs4140685
rs4140685 		2 161995569 intron variant G/T snv 0.35
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs4664446
rs4664446 		2 162053893 intron variant A/G snv 0.43
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs12617656
rs12617656 		0.925 0.200 2 161994637 intron variant T/C snv 0.35
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 2016 2016
dbSNP: rs201137953
rs201137953 		2 162039019 missense variant T/A;C snv 4.0E-06
CUI: C0021051
Disease: Immunologic Deficiency Syndromes
Immunologic Deficiency Syndromes 		Immune System Diseases 0.010 1.000 1 2000 2000
dbSNP: rs3788979
rs3788979 		0.925 0.080 2 162044379 intron variant C/T snv 0.14
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs3788979
rs3788979 		0.925 0.080 2 162044379 intron variant C/T snv 0.14
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs4664443
rs4664443 		1.000 0.080 2 162029379 intron variant A/G;T snv
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 2016 2016
dbSNP: rs7608798
rs7608798 		0.925 0.040 2 162033707 intron variant G/A snv 0.35
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders 		Mental Disorders 0.010 < 0.001 1 2015 2015
dbSNP: rs7608798
rs7608798 		0.925 0.040 2 162033707 intron variant G/A snv 0.35
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		Mental Disorders 0.010 1.000 1 2015 2015