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: 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: rs201191369
rs201191369 		1.000 11 78854232 missense variant C/T snv 7.9E-04 9.6E-04
CUI: C4225223
Disease: TREMOR, HEREDITARY ESSENTIAL, 5
TREMOR, HEREDITARY ESSENTIAL, 5 		0.700 1.000 1 2015 2015
dbSNP: rs201769315
rs201769315 		1.000 11 78668992 missense variant C/T snv 8.6E-04 1.1E-03
CUI: C4225223
Disease: TREMOR, HEREDITARY ESSENTIAL, 5
TREMOR, HEREDITARY ESSENTIAL, 5 		0.700 1.000 1 2015 2015
dbSNP: rs201995608
rs201995608 		1.000 11 78676361 missense variant C/T snv 4.3E-04 4.2E-04
CUI: C4225223
Disease: TREMOR, HEREDITARY ESSENTIAL, 5
TREMOR, HEREDITARY ESSENTIAL, 5 		0.700 1.000 1 2015 2015
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: rs538881762
rs538881762 		1.000 11 78726217 missense variant C/A;T snv 4.0E-06; 4.4E-04
CUI: C4225223
Disease: TREMOR, HEREDITARY ESSENTIAL, 5
TREMOR, HEREDITARY ESSENTIAL, 5 		0.800 1.000 1 2015 2015
dbSNP: rs556858741
rs556858741 		1.000 11 78729400 missense variant C/A;T snv 5.0E-06 7.0E-06
CUI: C4225223
Disease: TREMOR, HEREDITARY ESSENTIAL, 5
TREMOR, HEREDITARY ESSENTIAL, 5 		0.700 1.000 1 2015 2015
dbSNP: rs760852624
rs760852624 		1.000 11 79069787 missense variant C/G snv
CUI: C4225223
Disease: TREMOR, HEREDITARY ESSENTIAL, 5
TREMOR, HEREDITARY ESSENTIAL, 5 		0.700 1.000 1 2015 2015
dbSNP: rs763485258
rs763485258 		1.000 11 78708470 missense variant G/A;T snv 1.2E-05; 4.0E-06
CUI: C4225223
Disease: TREMOR, HEREDITARY ESSENTIAL, 5
TREMOR, HEREDITARY ESSENTIAL, 5 		0.800 1.000 1 2015 2015
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: 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: 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: 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: 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