TNIP1, TNFAIP3 interacting protein 1, 10318

N. diseases: 93; N. variants: 19
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: rs10036748
rs10036748 		0.752 0.360 5 151078585 intron variant C/A;T snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.830 1.000 6 2009 2017
dbSNP: rs2233278
rs2233278 		0.925 0.040 5 151087628 5 prime UTR variant G/C;T snv 4.8E-02
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.800 1.000 2 2012 2015
dbSNP: rs2233287
rs2233287 		0.925 0.160 5 151060536 intron variant G/A snv 0.11
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.800 1.000 1 2011 2011
dbSNP: rs960709
rs960709 		0.882 0.120 5 151081488 intron variant A/G;T snv
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.800 1.000 1 2013 2013
dbSNP: rs7708392
rs7708392 		0.732 0.400 5 151077924 intron variant G/C snv 0.44
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.730 1.000 6 2009 2018
dbSNP: rs10036748
rs10036748 		0.752 0.360 5 151078585 intron variant C/A;T snv
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.710 1.000 2 2015 2019
dbSNP: rs10463311
rs10463311 		1.000 0.080 5 151031274 intron variant C/T snv 0.66
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		Nutritional and Metabolic Diseases; Nervous System Diseases 0.710 1.000 2 2017 2018
dbSNP: rs1422673
rs1422673 		0.925 0.160 5 151059427 intron variant C/G;T snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.710 1.000 1 2012 2012
dbSNP: rs2233278
rs2233278 		0.925 0.040 5 151087628 5 prime UTR variant G/C;T snv 4.8E-02
CUI: C0263361
Disease: Psoriasis vulgaris
Psoriasis vulgaris 		Skin and Connective Tissue Diseases 0.700 1.000 2 2015 2018
dbSNP: rs6889239
rs6889239 		1.000 0.080 5 151078210 intron variant T/C snv 0.41
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.700 1.000 2 2015 2016
dbSNP: rs960709
rs960709 		0.882 0.120 5 151081488 intron variant A/G;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 2 2016 2019
dbSNP: rs1422673
rs1422673 		0.925 0.160 5 151059427 intron variant C/G;T snv
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis 		Neoplasms; Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs2233287
rs2233287 		0.925 0.160 5 151060536 intron variant G/A snv 0.11
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis 		Neoplasms; Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs2277940
rs2277940 		1.000 0.040 5 151029916 downstream gene variant T/C snv 7.9E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2011 2011
dbSNP: rs3762999
rs3762999 		1.000 0.040 5 151089865 intron variant C/T snv 0.49
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.700 1.000 1 2010 2010
dbSNP: rs3792783
rs3792783 		0.882 0.280 5 151076171 intron variant A/G snv 0.25
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.700 1.000 1 2019 2019
dbSNP: rs3792783
rs3792783 		0.882 0.280 5 151076171 intron variant A/G snv 0.25
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis 		Neoplasms; Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs3792785
rs3792785 		1.000 0.120 5 151072089 intron variant T/C snv 0.13
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis 		Neoplasms; Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs4958880
rs4958880 		0.851 0.160 5 151058916 intron variant C/A;G snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs4958880
rs4958880 		0.851 0.160 5 151058916 intron variant C/A;G snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs4958880
rs4958880 		0.851 0.160 5 151058916 intron variant C/A;G snv
CUI: C0027121
Disease: Myositis
Myositis 		Musculoskeletal Diseases; Nervous System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs4958880
rs4958880 		0.851 0.160 5 151058916 intron variant C/A;G snv
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.700 1.000 1 2019 2019
dbSNP: rs4958881
rs4958881 		0.827 0.280 5 151070675 intron variant T/C snv 0.21
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		Immune System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs4958881
rs4958881 		0.827 0.280 5 151070675 intron variant T/C snv 0.21
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases 		Immune System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs4958881
rs4958881 		0.827 0.280 5 151070675 intron variant T/C snv 0.21
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis 		Neoplasms; Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2012 2012