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: rs12098973
rs12098973 		11 131937277 intron variant A/G snv 0.33
CUI: C0523953
Disease: Cardiac troponin T measurement
Cardiac troponin T measurement 		0.800 1.000 1 2013 2013
dbSNP: rs1040103
rs1040103 		11 131572257 intron variant A/G snv 0.43
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs10750489
rs10750489 		1.000 0.040 11 131786445 intron variant C/G;T snv 0.91
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2011 2011
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: 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: rs11222652
rs11222652 		1.000 0.040 11 131463268 intron variant C/G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11222653
rs11222653 		1.000 0.040 11 131463704 intron variant A/C;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1169275
rs1169275 		11 131971373 intron variant C/A;T snv
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2018 2018
dbSNP: rs12222235
rs12222235 		11 132114436 intron variant C/T snv 0.29
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs12278021
rs12278021 		1.000 0.040 11 131462231 intron variant G/A snv 0.14
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs12419920
rs12419920 		1.000 0.040 11 131466286 intron variant C/T snv 0.23
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs12575010
rs12575010 		1.000 0.040 11 131474218 intron variant A/G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs12788343
rs12788343 		11 131583018 intron variant T/C snv 0.32
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs1449435
rs1449435 		11 132219023 intron variant G/A snv 0.37
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs1506662
rs1506662 		11 131607353 intron variant G/A snv 0.47
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
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: rs1625427
rs1625427 		11 132087399 intron variant T/C snv 0.31
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs1793639
rs1793639 		1.000 0.040 11 132061637 intron variant G/A snv 0.39
CUI: C0027092
Disease: Myopia
Myopia 		Eye Diseases 0.700 1.000 1 2016 2016
dbSNP: rs3099769
rs3099769 		11 132318528 intron variant G/A;C;T snv
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs35974940
rs35974940 		1.000 0.040 11 131375192 intron variant G/T snv 3.3E-02
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.700 1.000 1 2016 2016
dbSNP: rs4937627
rs4937627 		1.000 0.040 11 131481990 intron variant C/T snv 9.2E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7107326
rs7107326 		1.000 0.040 11 131462673 intron variant C/A;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
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: rs75038630
rs75038630 		11 131888434 intron variant C/A;G;T snv
CUI: C0015745
Disease: Feeding behaviors
Feeding behaviors 		Behavior and Behavior Mechanisms 0.700 1.000 1 2016 2016