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: 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: rs12201458
rs12201458
1.000 0.080 6 106194812 intron variant C/A snv 7.7E-02
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs12212740
rs12212740
1.000 0.080 6 106301433 intron variant G/A snv 8.3E-02
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2012 2012
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: rs1322178
rs1322178
1.000 0.080 6 106183905 intron variant C/T snv 0.15
Squamous cell carcinoma of esophagus
Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs1372169495
rs1372169495
1.000 6 106086585 missense variant G/A;C snv 6.3E-06; 6.3E-06
Pre B-cell acute lymphoblastic leukemia
0.010 1.000 1 2014 2014
dbSNP: rs2185379
rs2185379
1.000 0.080 6 106088378 missense variant G/A snv 3.8E-02 4.5E-02
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
Digestive System Diseases; Infections 0.010 1.000 1 2019 2019
dbSNP: rs2245214
rs2245214
0.827 0.240 6 106214866 intron variant C/G snv 0.42
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2245214
rs2245214
0.827 0.240 6 106214866 intron variant C/G snv 0.42
CUI: C0002871
Disease: Anemia
Anemia
Hemic and Lymphatic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2245214
rs2245214
0.827 0.240 6 106214866 intron variant C/G snv 0.42
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs2245214
rs2245214
0.827 0.240 6 106214866 intron variant C/G snv 0.42
CUI: C0029401
Disease: Osteitis Deformans
Osteitis Deformans
Musculoskeletal Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2245214
rs2245214
0.827 0.240 6 106214866 intron variant C/G snv 0.42
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
Neoplasms; Endocrine System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2245214
rs2245214
0.827 0.240 6 106214866 intron variant C/G snv 0.42
CUI: C1443892
Disease: Chronic Q Fever
Chronic Q Fever
Infections 0.010 1.000 1 2019 2019
dbSNP: rs3804329
rs3804329
1.000 0.080 6 106238552 intron variant A/G snv 0.15
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs3804329
rs3804329
1.000 0.080 6 106238552 intron variant A/G snv 0.15
Squamous cell carcinoma of esophagus
Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs473543
rs473543
0.925 0.080 6 106327811 upstream gene variant A/C;G snv
CUI: C3539878
Disease: Triple Negative Breast Neoplasms
Triple Negative Breast Neoplasms
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs473543
rs473543
0.925 0.080 6 106327811 upstream gene variant A/C;G snv
CUI: C4722518
Disease: Triple-Negative Breast Carcinoma
Triple-Negative Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
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