Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3748067
rs3748067
IL17A
0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.030 1.000 3 2015 2017
dbSNP: rs3748067
rs3748067
IL17A
0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		0.030 1.000 3 2015 2017
dbSNP: rs3819024
rs3819024
IL17A
0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.030 0.667 3 2015 2019
dbSNP: rs8193036
rs8193036
IL17A
0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.030 1.000 3 2015 2016
dbSNP: rs8193036
rs8193036
IL17A
0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.030 0.333 3 2015 2019
dbSNP: rs8193037
rs8193037
IL17A
0.752 0.320 6 52186311 upstream gene variant G/A;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.030 1.000 3 2011 2016
dbSNP: rs10484879
rs10484879
IL17A
0.827 0.160 6 52187159 intron variant G/A;T snv
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.020 1.000 2 2015 2018
dbSNP: rs148704956
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.020 1.000 2 2014 2016
dbSNP: rs148704956
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis 		0.020 1.000 2 2012 2015
dbSNP: rs148704956
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.020 1.000 2 2014 2016
dbSNP: rs2275913
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.020 1.000 2 2014 2017
dbSNP: rs2275913
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary 		0.020 1.000 2 2013 2016
dbSNP: rs2275913
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0006271
Disease: Bronchiolitis
Bronchiolitis 		0.020 1.000 2 2010 2018
dbSNP: rs2275913
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0029400
Disease: Osteitis
Osteitis 		0.020 1.000 2 2017 2017
dbSNP: rs2275913
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.020 1.000 2 2017 2018
dbSNP: rs2275913
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.020 1.000 2 2015 2016
dbSNP: rs2275913
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.020 0.500 2 2014 2015
dbSNP: rs2275913
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		0.020 1.000 2 2010 2018
dbSNP: rs3748067
rs3748067
IL17A
0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		0.020 1.000 2 2016 2017
dbSNP: rs3748067
rs3748067
IL17A
0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.020 1.000 2 2018 2019
dbSNP: rs3748067
rs3748067
IL17A
0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02
CUI: C0006309
Disease: Brucellosis
Brucellosis 		0.020 1.000 2 2013 2019
dbSNP: rs4711998
rs4711998
IL17A
0.708 0.360 6 52185555 upstream gene variant A/G snv 0.64
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.020 1.000 2 2016 2016
dbSNP: rs4711998
rs4711998
IL17A
0.708 0.360 6 52185555 upstream gene variant A/G snv 0.64
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.020 < 0.001 2 2015 2017
dbSNP: rs4711998
rs4711998
IL17A
0.708 0.360 6 52185555 upstream gene variant A/G snv 0.64
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.020 1.000 2 2016 2016
dbSNP: rs4711998
rs4711998
IL17A
0.708 0.360 6 52185555 upstream gene variant A/G snv 0.64
CUI: C0006309
Disease: Brucellosis
Brucellosis 		0.020 1.000 2 2013 2019