TRIM26, tripartite motif containing 26, 7726

N. diseases: 31; 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: rs2021722
rs2021722 		0.851 0.040 6 30206354 intron variant C/A;T snv 0.24
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.800 1.000 2 2011 2013
dbSNP: rs2523722
rs2523722 		1.000 0.040 6 30197496 intron variant C/T snv 0.23
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.800 1.000 2 2012 2013
dbSNP: rs2021722
rs2021722 		0.851 0.040 6 30206354 intron variant C/A;T snv 0.24
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.800 1.000 1 2013 2013
dbSNP: rs116408368
rs116408368 		1.000 0.040 6 30202733 intron variant T/C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 2 2017 2019
dbSNP: rs4711211
rs4711211 		1.000 0.120 6 30195032 intron variant A/G snv 0.17
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 2 2007 2009
dbSNP: rs1117490
rs1117490 		0.925 0.080 6 30202733 intron variant T/C snv 0.24
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1117490
rs1117490 		0.925 0.080 6 30202733 intron variant T/C snv 0.24
CUI: C0741260
Disease: Adult onset asthma
Adult onset asthma 		0.700 1.000 1 2019 2019
dbSNP: rs114265779
rs114265779 		1.000 0.080 6 30213844 upstream gene variant C/T snv
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases 0.700 1.000 1 2019 2019
dbSNP: rs116408368
rs116408368 		1.000 0.040 6 30202733 intron variant T/C snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs116418332
rs116418332 		0.925 0.080 6 30193759 intron variant G/A snv
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.700 1.000 1 2017 2017
dbSNP: rs116418332
rs116418332 		0.925 0.080 6 30193759 intron variant G/A snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.700 1.000 1 2017 2017
dbSNP: rs11967808
rs11967808 		1.000 0.040 6 30211411 intron variant G/C snv 3.2E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo 		Skin and Connective Tissue Diseases 0.700 1.000 1 2010 2010
dbSNP: rs2021722
rs2021722 		0.851 0.040 6 30206354 intron variant C/A;T snv 0.24
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs2021722
rs2021722 		0.851 0.040 6 30206354 intron variant C/A;T snv 0.24
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs2021722
rs2021722 		0.851 0.040 6 30206354 intron variant C/A;T snv 0.24
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs2072107
rs2072107 		1.000 6 30199158 splice region variant G/A snv 0.12
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2010 2010
dbSNP: rs2072107
rs2072107 		1.000 6 30199158 splice region variant G/A snv 0.12
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2010 2010
dbSNP: rs2072107
rs2072107 		1.000 6 30199158 splice region variant G/A snv 0.12
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2010 2010
dbSNP: rs2072107
rs2072107 		1.000 6 30199158 splice region variant G/A snv 0.12
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2010 2010
dbSNP: rs2844775
rs2844775 		6 30211645 intron variant G/A snv 0.19
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		Behavior and Behavior Mechanisms 0.700 1.000 1 2014 2014
dbSNP: rs2844775
rs2844775 		6 30211645 intron variant G/A snv 0.19
CUI: C0002957
Disease: Anger
Anger 		Behavior and Behavior Mechanisms 0.700 1.000 1 2014 2014
dbSNP: rs117565607
rs117565607 		1.000 0.120 6 30204594 intron variant T/A snv 2.3E-03
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2018 2018