ATG5, autophagy related 5, 9474

N. diseases: 282; N. variants: 36
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: rs9373839
rs9373839
0.882 0.080 6 106207742 intron variant T/C snv 0.15
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
Skin and Connective Tissue Diseases 0.700 1.000 1 2014 2014
dbSNP: rs9373839
rs9373839
0.882 0.080 6 106207742 intron variant T/C snv 0.15
CUI: C0748540
Disease: Scleroderma, Limited
Scleroderma, Limited
Skin and Connective Tissue Diseases 0.700 1.000 1 2014 2014
dbSNP: rs9373839
rs9373839
0.882 0.080 6 106207742 intron variant T/C snv 0.15
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs1010273
rs1010273
0.882 0.120 6 106107150 synonymous variant G/A snv 9.7E-02 7.7E-02
Hepatitis B Virus-Related Hepatocellular Carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs1010273
rs1010273
0.882 0.120 6 106107150 synonymous variant G/A snv 9.7E-02 7.7E-02
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
Digestive System Diseases; Infections 0.010 1.000 1 2019 2019
dbSNP: rs1010273
rs1010273
0.882 0.120 6 106107150 synonymous variant G/A snv 9.7E-02 7.7E-02
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs1040411
rs1040411
1.000 0.120 6 106150148 intron variant G/A snv 0.47
CUI: C2939419
Disease: Secondary Neoplasm
Secondary Neoplasm
Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs1040411
rs1040411
1.000 0.120 6 106150148 intron variant G/A snv 0.47
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs1040411
rs1040411
1.000 0.120 6 106150148 intron variant G/A snv 0.47
CUI: C0220644
Disease: Childhood Hodgkin Lymphoma
Childhood Hodgkin Lymphoma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1312391542
rs1312391542
0.925 0.120 6 106104897 missense variant G/A;T snv
CUI: C1332201
Disease: Adult Diffuse Large B-Cell Lymphoma
Adult Diffuse Large B-Cell Lymphoma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2009 2009
dbSNP: rs1312391542
rs1312391542
0.925 0.120 6 106104897 missense variant G/A;T snv
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
Diffuse Large B-Cell Lymphoma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2009 2009
dbSNP: rs28701841
rs28701841
0.827 0.120 6 106082455 intron variant G/A snv 7.6E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs28701841
rs28701841
0.827 0.120 6 106082455 intron variant G/A snv 7.6E-02
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs28701841
rs28701841
0.827 0.120 6 106082455 intron variant G/A snv 7.6E-02
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs28701841
rs28701841
0.827 0.120 6 106082455 intron variant G/A snv 7.6E-02
CUI: C0033860
Disease: Psoriasis
Psoriasis
Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs28701841
rs28701841
0.827 0.120 6 106082455 intron variant G/A snv 7.6E-02
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
Musculoskeletal Diseases 0.700 1.000 1 2016 2016
dbSNP: rs4946728
rs4946728
1.000 0.120 6 106142488 intron variant A/C snv 0.72
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs4946728
rs4946728
1.000 0.120 6 106142488 intron variant A/C snv 0.72
CUI: C0220644
Disease: Childhood Hodgkin Lymphoma
Childhood Hodgkin Lymphoma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs4946728
rs4946728
1.000 0.120 6 106142488 intron variant A/C snv 0.72
CUI: C2939419
Disease: Secondary Neoplasm
Secondary Neoplasm
Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs757085537
rs757085537
0.851 0.160 6 106105356 missense variant C/T snv 7.0E-06
Activated B-cell type diffuse large B-cell lymphoma
0.010 1.000 1 2014 2014
dbSNP: rs757085537
rs757085537
0.851 0.160 6 106105356 missense variant C/T snv 7.0E-06
Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type
0.010 1.000 1 2017 2017
dbSNP: rs757085537
rs757085537
0.851 0.160 6 106105356 missense variant C/T snv 7.0E-06
Malignant lymphoma - lymphoplasmacytic
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs757085537
rs757085537
0.851 0.160 6 106105356 missense variant C/T snv 7.0E-06
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs757085537
rs757085537
0.851 0.160 6 106105356 missense variant C/T snv 7.0E-06
CUI: C0024419
Disease: Waldenstrom Macroglobulinemia
Waldenstrom Macroglobulinemia
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs802791
rs802791
0.851 0.160 6 106121395 intron variant T/C snv 0.75
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
Skin and Connective Tissue Diseases 0.700 1.000 1 2019 2019