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: 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: 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: 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: 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: 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: rs12577093
rs12577093 		1.000 0.040 11 79346052 intron variant C/A;T snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs2187172
rs2187172 		1.000 0.080 11 79098201 intron variant G/A;C;T snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.700 1.000 1 2017 2017
dbSNP: rs533870
rs533870 		1.000 0.040 11 79160857 intron variant A/C;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
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: rs7127580
rs7127580 		1.000 0.040 11 79433812 intron variant C/A;G snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2014 2014
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: 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: rs865922915
rs865922915 		1.000 0.040 11 78669621 missense variant G/A snv 1.4E-05
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2018 2018
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: 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: rs754333774
rs754333774 		1.000 0.040 11 79402363 intron variant C/T snv 3.3E-04
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.010 1.000 1 2016 2016
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: 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: 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: rs1938946
rs1938946 		1.000 0.040 11 79161716 intron variant T/C snv 3.1E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs12577328
rs12577328 		1.000 0.040 11 79382430 intron variant C/G snv 8.3E-02
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