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: 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: 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: 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: rs12788335
rs12788335 		1.000 0.040 11 79158052 intron variant C/T snv 0.18
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1511237
rs1511237 		1.000 0.040 11 79403640 intron variant C/T snv 0.11
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: 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: 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: 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: 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: rs471435
rs471435 		1.000 0.040 11 79366701 intron variant T/C snv 0.17
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
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: 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: rs536962
rs536962 		1.000 0.040 11 79357399 intron variant A/G snv 0.79
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs550547
rs550547 		1.000 0.040 11 79157534 intron variant A/T snv 0.94
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs556857
rs556857 		1.000 0.040 11 79357503 intron variant T/C snv 0.79
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
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: rs575257
rs575257 		1.000 0.040 11 79158025 intron variant G/A snv 0.49
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7108878
rs7108878 		1.000 0.040 11 79396763 intron variant T/G snv 0.10
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2014 2014
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