IL17A, interleukin 17A, 3605

N. diseases: 1074; 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: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.100 0.857 14 2012 2018
dbSNP: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
Digestive System Diseases; Neoplasms 0.100 0.857 14 2012 2018
dbSNP: rs3748067
rs3748067
0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.080 0.750 8 2012 2018
dbSNP: rs3748067
rs3748067
0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
Digestive System Diseases; Neoplasms 0.080 0.750 8 2012 2018
dbSNP: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.070 0.857 7 2015 2020
dbSNP: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.060 1.000 6 2015 2017
dbSNP: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.060 1.000 6 2010 2018
dbSNP: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C4048328
Disease: cervical cancer
cervical cancer
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.060 1.000 6 2015 2017
dbSNP: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.060 1.000 6 2015 2017
dbSNP: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.050 1.000 5 2014 2019
dbSNP: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.050 1.000 5 2015 2019
dbSNP: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
Infections 0.050 0.600 5 2013 2017
dbSNP: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
Digestive System Diseases 0.050 1.000 5 2008 2014
dbSNP: rs148704956
rs148704956
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
Digestive System Diseases; Neoplasms 0.040 1.000 4 2010 2018
dbSNP: rs148704956
rs148704956
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.040 1.000 4 2010 2018
dbSNP: rs148704956
rs148704956
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.040 1.000 4 2014 2018
dbSNP: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.040 1.000 4 2014 2016
dbSNP: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee
Musculoskeletal Diseases 0.040 1.000 4 2019 2019
dbSNP: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.040 1.000 4 2014 2016
dbSNP: rs3748067
rs3748067
0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.040 1.000 4 2015 2016
dbSNP: rs148704956
rs148704956
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06
Malignant neoplasm of colon and/or rectum
0.030 1.000 3 2014 2018
dbSNP: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
Malignant neoplasm of colon and/or rectum
0.030 1.000 3 2014 2017
dbSNP: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.030 1.000 3 2016 2019
dbSNP: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0031099
Disease: Periodontitis
Periodontitis
Stomatognathic Diseases 0.030 1.000 3 2013 2017
dbSNP: rs3748067
rs3748067
0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02
CUI: C4048328
Disease: cervical cancer
cervical cancer
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.030 1.000 3 2015 2017