TRAP1, TNF receptor associated protein 1, 10131

N. diseases: 90; N. variants: 18
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: rs12597773
rs12597773
1.000 0.040 16 3714708 intron variant G/A;C snv
CUI: C0018939
Disease: Hematological Disease
Hematological Disease
Hemic and Lymphatic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs12597773
rs12597773
1.000 0.040 16 3714708 intron variant G/A;C snv
CUI: C0149745
Disease: Oral Ulcer
Oral Ulcer
Stomatognathic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1635404
rs1635404
16 3697041 intron variant G/T snv 0.77
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2019 2019
dbSNP: rs1639150
rs1639150
0.925 0.120 16 3697203 intron variant C/T snv 0.49
CUI: C0018939
Disease: Hematological Disease
Hematological Disease
Hemic and Lymphatic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1639150
rs1639150
0.925 0.120 16 3697203 intron variant C/T snv 0.49
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1639150
rs1639150
0.925 0.120 16 3697203 intron variant C/T snv 0.49
CUI: C0149745
Disease: Oral Ulcer
Oral Ulcer
Stomatognathic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2072379
rs2072379
0.925 0.120 16 3688886 intron variant C/T snv 0.75
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2072379
rs2072379
0.925 0.120 16 3688886 intron variant C/T snv 0.75
CUI: C0149745
Disease: Oral Ulcer
Oral Ulcer
Stomatognathic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2072379
rs2072379
0.925 0.120 16 3688886 intron variant C/T snv 0.75
CUI: C0018939
Disease: Hematological Disease
Hematological Disease
Hemic and Lymphatic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2158962
rs2158962
1.000 0.040 16 3688026 intron variant A/G snv 0.57
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs3751842
rs3751842
1.000 0.040 16 3664610 3 prime UTR variant C/G;T snv
CUI: C0149745
Disease: Oral Ulcer
Oral Ulcer
Stomatognathic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs3751842
rs3751842
1.000 0.040 16 3664610 3 prime UTR variant C/G;T snv
CUI: C0018939
Disease: Hematological Disease
Hematological Disease
Hemic and Lymphatic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs3794701
rs3794701
1.000 0.080 16 3680577 intron variant A/G;T snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs56340469
rs56340469
16 3696768 intron variant C/G snv 4.4E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs6500550
rs6500550
16 3696240 intron variant C/G;T snv
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs6500550
rs6500550
16 3696240 intron variant C/G;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2016 2016
dbSNP: rs6500550
rs6500550
16 3696240 intron variant C/G;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs6500550
rs6500550
16 3696240 intron variant C/G;T snv
CUI: C0857490
Disease: Granulocyte count
Granulocyte count
0.700 1.000 1 2016 2016
dbSNP: rs6500550
rs6500550
16 3696240 intron variant C/G;T snv
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1.000 1 2016 2016
dbSNP: rs6500552
rs6500552
1.000 0.080 16 3709392 intron variant T/A;C snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs7203664
rs7203664
16 3678707 intron variant T/C snv 0.68
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2019 2019
dbSNP: rs8055172
rs8055172
1.000 0.080 16 3699224 intron variant T/C snv 0.22
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs977605156
rs977605156
0.925 0.080 16 3656127 missense variant G/A snv 7.0E-06
CUI: C0011570
Disease: Mental Depression
Mental Depression
Behavior and Behavior Mechanisms 0.010 1.000 1 2015 2015
dbSNP: rs977605156
rs977605156
0.925 0.080 16 3656127 missense variant G/A snv 7.0E-06
CUI: C0344315
Disease: Depressed mood
Depressed mood
Behavior and Behavior Mechanisms 0.010 1.000 1 2015 2015
dbSNP: rs977605156
rs977605156
0.925 0.080 16 3656127 missense variant G/A snv 7.0E-06
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
Mental Disorders 0.010 1.000 1 2015 2015