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: rs199687168
rs199687168 		1.000 11 78701718 missense variant C/T snv 4.9E-04 6.5E-04
CUI: C4225223
Disease: TREMOR, HEREDITARY ESSENTIAL, 5
TREMOR, HEREDITARY ESSENTIAL, 5 		0.700 0
dbSNP: rs375681722
rs375681722 		1.000 11 78702289 missense variant C/T snv 5.6E-05 2.5E-04
CUI: C4225223
Disease: TREMOR, HEREDITARY ESSENTIAL, 5
TREMOR, HEREDITARY ESSENTIAL, 5 		0.800 0
dbSNP: rs770111861
rs770111861 		1.000 11 78702010 missense variant T/G snv 9.2E-05 8.4E-05
CUI: C4225223
Disease: TREMOR, HEREDITARY ESSENTIAL, 5
TREMOR, HEREDITARY ESSENTIAL, 5 		0.700 0
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: 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: 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: rs499949
rs499949 		11 79282162 intron variant C/T snv 0.58
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
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: 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: 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: 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: 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
dbSNP: rs11237805
rs11237805 		1.000 0.040 11 79367625 intron variant A/G;T snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs11237815
rs11237815 		1.000 0.040 11 79379756 intron variant A/G snv 0.10
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs11237820
rs11237820 		1.000 0.040 11 79393621 intron variant G/A snv 8.7E-02
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs11237821
rs11237821 		1.000 0.040 11 79395760 intron variant C/A;T snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs12275195
rs12275195 		1.000 0.040 11 79394755 intron variant A/C snv 0.12
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs12277834
rs12277834 		1.000 0.040 11 79389112 intron variant C/A;T snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs12279388
rs12279388 		1.000 0.040 11 79356629 intron variant A/G snv 0.15
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs12289486
rs12289486 		1.000 0.040 11 79381483 intron variant C/T snv 8.4E-02
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2014 2014