DPP6, dipeptidyl peptidase like 6, 1804

N. diseases: 71; N. variants: 24
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: rs10260404
rs10260404 		0.925 0.080 7 154513713 intron variant T/C snv 0.35
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		Nutritional and Metabolic Diseases; Nervous System Diseases 0.820 0.667 3 2008 2011
dbSNP: rs786205143
rs786205143 		1.000 7 154794095 missense variant A/C snv
CUI: C4225375
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 33
MENTAL RETARDATION, AUTOSOMAL DOMINANT 33 		0.800 0
dbSNP: rs10251943
rs10251943 		1.000 0.040 7 154189530 intron variant G/A;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs10280963
rs10280963 		1.000 0.040 7 154189483 intron variant A/C snv 0.41
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11243354
rs11243354 		1.000 0.040 7 154587524 intron variant T/C snv 0.27
CUI: C0877015
Disease: Pelvic Organ Prolapse
Pelvic Organ Prolapse 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2015 2015
dbSNP: rs118189482
rs118189482 		1.000 0.040 7 154668950 intron variant C/T snv 1.0E-02
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.700 1.000 1 2015 2015
dbSNP: rs118189482
rs118189482 		1.000 0.040 7 154668950 intron variant C/T snv 1.0E-02
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2015 2015
dbSNP: rs11975478
rs11975478 		1.000 0.040 7 154187872 intron variant C/T snv 0.24
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs12671878
rs12671878 		1.000 0.040 7 153861864 intergenic variant C/A;T snv
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs2110267
rs2110267 		1.000 0.040 7 153838604 intergenic variant C/G snv 0.32
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs2192271
rs2192271 		1.000 0.040 7 153852211 intergenic variant C/T snv 0.18
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs2316527
rs2316527 		1.000 0.080 7 154830747 intron variant G/A snv 7.5E-02
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs6464375
rs6464375 		0.925 0.120 7 153928758 intron variant C/T snv 6.7E-02
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.700 1.000 1 2010 2010
dbSNP: rs6464375
rs6464375 		0.925 0.120 7 153928758 intron variant C/T snv 6.7E-02
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas 		Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.700 1.000 1 2010 2010
dbSNP: rs6464387
rs6464387 		1.000 0.040 7 154195084 intron variant C/A;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs6947495
rs6947495 		1.000 0.040 7 153855979 intergenic variant A/G;T snv
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs6955717
rs6955717 		1.000 0.040 7 154194756 intron variant T/C snv 0.20
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs6975879
rs6975879 		1.000 0.080 7 154612554 intron variant A/G snv 0.40
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs73169094
rs73169094 		7 154888650 intron variant C/G snv 1.9E-02
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2017 2017
dbSNP: rs7811481
rs7811481 		1.000 0.040 7 154196075 intron variant G/A snv 0.37
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs606231226
rs606231226 		1.000 0.080 7 154305155 5 prime UTR variant C/T snv
CUI: C2751829
Disease: Ventricular Fibrillation, Paroxysmal Familial, 2
Ventricular Fibrillation, Paroxysmal Familial, 2 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 0
dbSNP: rs10260404
rs10260404 		0.925 0.080 7 154513713 intron variant T/C snv 0.35
CUI: C1862941
Disease: Amyotrophic Lateral Sclerosis, Sporadic
Amyotrophic Lateral Sclerosis, Sporadic 		Nutritional and Metabolic Diseases; Nervous System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs17174381
rs17174381 		1.000 0.080 7 154381147 intron variant C/A snv 3.4E-02
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		Nutritional and Metabolic Diseases; Nervous System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs2110267
rs2110267 		1.000 0.040 7 153838604 intergenic variant C/G snv 0.32
CUI: C0021125
Disease: Impulsive Behavior
Impulsive Behavior 		Behavior and Behavior Mechanisms 0.010 1.000 1 2013 2013
dbSNP: rs2110267
rs2110267 		1.000 0.040 7 153838604 intergenic variant C/G snv 0.32
CUI: C0424295
Disease: Hyperactive behavior
Hyperactive behavior 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 1.000 1 2013 2013