NTM, neurotrimin, 50863

N. diseases: 58; N. variants: 27
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: rs11222647
rs11222647
1.000 0.040 11 131461593 intron variant G/A snv 6.0E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11222631
rs11222631
1.000 0.040 11 131456474 intron variant A/T snv 6.0E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7481514
rs7481514
1.000 0.040 11 131422069 intron variant A/G;T snv
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle
Eye Diseases 0.010 1.000 1 2012 2012
dbSNP: rs1550972
rs1550972
1.000 0.040 11 131421915 intron variant A/G snv 0.70
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs1550972
rs1550972
1.000 0.040 11 131421915 intron variant A/G snv 0.70
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs7108020
rs7108020
11 131419926 intron variant C/A;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs35974940
rs35974940
1.000 0.040 11 131375192 intron variant G/T snv 3.3E-02
Attention deficit hyperactivity disorder
Mental Disorders 0.700 1.000 1 2016 2016