TENM2, teneurin transmembrane protein 2, 57451

N. diseases: 44; N. variants: 33
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: rs10067798
rs10067798 		5 167413686 intron variant T/A snv 0.44
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs10462889
rs10462889 		5 167239713 intergenic variant G/A;C snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs12654709
rs12654709 		5 167456618 intron variant A/G snv 0.37
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs2973662
rs2973662 		5 167783467 intron variant A/G snv 0.98
CUI: C2699541
Disease: Cytokine Measurement
Cytokine Measurement 		0.800 1.000 1 2012 2012
dbSNP: rs32421
rs32421 		5 167935411 intron variant A/T snv 0.37
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs42210
rs42210 		5 166981783 intergenic variant G/A;C;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs4869022
rs4869022 		5 167239649 intergenic variant T/A;G snv 0.66
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs4869058
rs4869058 		5 167565242 intron variant T/A snv 0.57
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs6867056
rs6867056 		5 168108023 intron variant G/T snv 0.18
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs72827369
rs72827369 		5 167244178 intergenic variant T/C snv 0.25
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs73803919
rs73803919 		5 167648655 intron variant G/A snv 4.4E-04
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs9647570
rs9647570 		5 167943258 intron variant T/A;G snv
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2014 2014
dbSNP: rs172137
rs172137 		0.925 0.120 5 167604857 intron variant G/A;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs172137
rs172137 		0.925 0.120 5 167604857 intron variant G/A;T snv
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs2937582
rs2937582 		0.925 0.040 5 167038003 intergenic variant A/G snv 0.64
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs2937582
rs2937582 		0.925 0.040 5 167038003 intergenic variant A/G snv 0.64
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs6885116
rs6885116 		0.925 0.040 5 168216540 intron variant A/G snv 0.14
CUI: C0031099
Disease: Periodontitis
Periodontitis 		Stomatognathic Diseases 0.700 1.000 1 2012 2012
dbSNP: rs6885116
rs6885116 		0.925 0.040 5 168216540 intron variant A/G snv 0.14
CUI: C0600298
Disease: Periodontosis
Periodontosis 		Stomatognathic Diseases 0.700 1.000 1 2012 2012
dbSNP: rs10035359
rs10035359 		1.000 0.040 5 167575396 intron variant C/T snv 5.3E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs10045595
rs10045595 		1.000 0.080 5 167802999 intron variant T/G snv 0.36
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs10475853
rs10475853 		1.000 0.040 5 167576564 intron variant G/T snv 0.64
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11134465
rs11134465 		1.000 0.040 5 167610929 intron variant G/A snv 0.52
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11738133
rs11738133 		1.000 0.040 5 167605088 intron variant C/T snv 0.51
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11742502
rs11742502 		1.000 0.040 5 167585160 intron variant C/T snv 0.52
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs12517217
rs12517217 		1.000 0.040 5 167610002 intron variant C/T snv 1.6E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017