TENM4, teneurin transmembrane protein 4, 26011

N. diseases: 44; N. variants: 52
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: rs1151200
rs1151200 		11 79281641 intron variant T/C snv 0.50
CUI: C0005612
Disease: Birth Weight
Birth Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2012 2012
dbSNP: rs1151200
rs1151200 		11 79281641 intron variant T/C snv 0.50
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs12275127
rs12275127 		11 79418571 intron variant T/A snv 0.18
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs499949
rs499949 		11 79282162 intron variant C/T snv 0.58
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs12576775
rs12576775 		0.827 0.080 11 79366149 intron variant A/G snv 0.15
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.820 1.000 7 2011 2018
dbSNP: rs12576775
rs12576775 		0.827 0.080 11 79366149 intron variant A/G snv 0.15
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs12576775
rs12576775 		0.827 0.080 11 79366149 intron variant A/G snv 0.15
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs12576775
rs12576775 		0.827 0.080 11 79366149 intron variant A/G snv 0.15
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs12576775
rs12576775 		0.827 0.080 11 79366149 intron variant A/G snv 0.15
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs12576775
rs12576775 		0.827 0.080 11 79366149 intron variant A/G snv 0.15
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.800 1.000 1 2013 2013
dbSNP: rs12290811
rs12290811 		0.882 0.120 11 79372576 intron variant T/A snv 0.18
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.800 1.000 1 2014 2014
dbSNP: rs12290811
rs12290811 		0.882 0.120 11 79372576 intron variant T/A snv 0.18
CUI: C0006012
Disease: Borderline Personality Disorder
Borderline Personality Disorder 		Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs12290811
rs12290811 		0.882 0.120 11 79372576 intron variant T/A snv 0.18
CUI: C0006287
Disease: Bronchopulmonary Dysplasia
Bronchopulmonary Dysplasia 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases 0.010 1.000 1 2014 2014
dbSNP: rs17138230
rs17138230 		0.925 0.080 11 79364808 intron variant A/T snv 0.16
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs17138230
rs17138230 		0.925 0.080 11 79364808 intron variant A/T snv 0.16
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7932890
rs7932890 		0.925 0.080 11 79357349 intron variant A/G snv 0.19
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs7932890
rs7932890 		0.925 0.080 11 79357349 intron variant A/G snv 0.19
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs17138171
rs17138171 		1.000 0.040 11 79351885 intron variant T/A;C snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 2 2013 2014
dbSNP: rs1944449
rs1944449 		1.000 0.040 11 79372205 intron variant C/T snv 0.18
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 2 2013 2014
dbSNP: rs10501434
rs10501434 		1.000 0.040 11 79159052 intron variant A/C;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs10501439
rs10501439 		1.000 0.040 11 79374802 intron variant A/G snv 0.18
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs10751301
rs10751301 		1.000 0.080 11 78983593 intron variant C/G snv 0.40
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 2011 2011
dbSNP: rs10793371
rs10793371 		1.000 0.040 11 79157391 intron variant T/C snv 0.81
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11237796
rs11237796 		1.000 0.040 11 79348399 intron variant A/G snv 0.16
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs11237799
rs11237799 		1.000 0.040 11 79356427 intron variant A/C;T snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2014 2014