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: 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: C0042384
Disease: Vasculitis
Vasculitis
Cardiovascular Diseases 0.010 1.000 1 2010 2010
dbSNP: rs10036748
rs10036748
0.752 0.360 5 151078585 intron variant C/A;T snv
CUI: C0027697
Disease: Nephritis
Nephritis
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2010 2010
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: 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: 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: rs7708392
rs7708392
0.732 0.400 5 151077924 intron variant G/C snv 0.44
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2011 2011
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: rs10036748
rs10036748
0.752 0.360 5 151078585 intron variant C/A;T snv
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs10036748
rs10036748
0.752 0.360 5 151078585 intron variant C/A;T snv
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
Skin and Connective Tissue Diseases 0.010 1.000 1 2012 2012
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: 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: 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: 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
dbSNP: rs7708392
rs7708392
0.732 0.400 5 151077924 intron variant G/C snv 0.44
CUI: C0024143
Disease: Lupus Nephritis
Lupus Nephritis
Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Male Urogenital Diseases; Immune System Diseases 0.020 1.000 2 2013 2018
dbSNP: rs3792783
rs3792783
0.882 0.280 5 151076171 intron variant A/G snv 0.25
CUI: C0151449
Disease: Primary Sjögren's syndrome
Primary Sjögren's syndrome
Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases 0.010 1.000 1 2013 2013
dbSNP: rs4958881
rs4958881
0.827 0.280 5 151070675 intron variant T/C snv 0.21
CUI: C0024143
Disease: Lupus Nephritis
Lupus Nephritis
Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Male Urogenital Diseases; Immune System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs4958881
rs4958881
0.827 0.280 5 151070675 intron variant T/C snv 0.21
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs4958881
rs4958881
0.827 0.280 5 151070675 intron variant T/C snv 0.21
CUI: C0027697
Disease: Nephritis
Nephritis
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2013 2013
dbSNP: rs6579837
rs6579837
1.000 0.200 5 151055333 intron variant G/T snv 0.11
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome
Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases 0.700 1.000 1 2013 2013