TNIK, TRAF2 and NCK interacting kinase, 23043

N. diseases: 83; N. variants: 11
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: rs115419280
rs115419280 		3 171131724 intron variant A/C snv 2.3E-02
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 1 2016 2016
dbSNP: rs11923305
rs11923305 		3 171400381 intron variant A/G snv 0.62
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs12635553
rs12635553 		3 171395925 intron variant A/T snv 0.50
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs13315469
rs13315469 		3 171142104 intron variant A/G snv 0.32
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs150394119
rs150394119 		3 171403444 intron variant G/A snv 6.2E-02
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		Behavior and Behavior Mechanisms 0.700 1.000 1 2015 2015
dbSNP: rs150394119
rs150394119 		3 171403444 intron variant G/A snv 6.2E-02
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2015 2015
dbSNP: rs16855732
rs16855732 		3 171063141 3 prime UTR variant A/G snv 2.4E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases 		Cardiovascular Diseases 0.700 1.000 1 2016 2016
dbSNP: rs6444970
rs6444970 		1.000 0.040 3 171192653 intron variant T/C snv 0.71
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs6809184
rs6809184 		1.000 0.120 3 171170409 intron variant C/T snv 6.2E-02
CUI: C0338451
Disease: Frontotemporal dementia
Frontotemporal dementia 		Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs9810566
rs9810566 		0.925 0.040 3 171153189 intron variant C/A;G snv
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2017 2017
dbSNP: rs9810566
rs9810566 		0.925 0.040 3 171153189 intron variant C/A;G snv
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2017 2017
dbSNP: rs886037841
rs886037841 		1.000 3 171188803 stop gained G/A snv
CUI: C4310755
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 54
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 54 		0.700 0
dbSNP: rs2422299
rs2422299 		0.882 0.080 3 171440696 intron variant C/G;T snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2016 2016
dbSNP: rs2422299
rs2422299 		0.882 0.080 3 171440696 intron variant C/G;T snv
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2016 2016
dbSNP: rs2422299
rs2422299 		0.882 0.080 3 171440696 intron variant C/G;T snv
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2016 2016