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: 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: rs10484879
rs10484879
IL17A
0.827 0.160 6 52187159 intron variant G/A;T snv
CUI: C0007113
Disease: Rectal Carcinoma
Rectal Carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs10484879
rs10484879
IL17A
0.827 0.160 6 52187159 intron variant G/A;T snv
CUI: C0031099
Disease: Periodontitis
Periodontitis 		0.010 1.000 1 2013 2013
dbSNP: rs10484879
rs10484879
IL17A
0.827 0.160 6 52187159 intron variant G/A;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2018 2018
dbSNP: rs10484879
rs10484879
IL17A
0.827 0.160 6 52187159 intron variant G/A;T snv
CUI: C2936258
Disease: Peri-Implantitis
Peri-Implantitis 		0.010 1.000 1 2013 2013
dbSNP: rs3804513
rs3804513
IL17A
0.851 0.080 6 52188399 intron variant A/T snv 2.4E-02
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.010 1.000 1 2013 2013
dbSNP: rs3804513
rs3804513
IL17A
0.851 0.080 6 52188399 intron variant A/T snv 2.4E-02
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs3804513
rs3804513
IL17A
0.851 0.080 6 52188399 intron variant A/T snv 2.4E-02
CUI: C0007113
Disease: Rectal Carcinoma
Rectal Carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs3804513
rs3804513
IL17A
0.851 0.080 6 52188399 intron variant A/T snv 2.4E-02
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.010 1.000 1 2019 2019
dbSNP: rs3819025
rs3819025
IL17A
0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2012 2012
dbSNP: rs3819025
rs3819025
IL17A
0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.010 1.000 1 2012 2012
dbSNP: rs3819025
rs3819025
IL17A
0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.010 < 0.001 1 2015 2015
dbSNP: rs3819025
rs3819025
IL17A
0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2012 2012
dbSNP: rs3819025
rs3819025
IL17A
0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
Henoch-Schoenlein Purpura 		0.010 1.000 1 2016 2016
dbSNP: rs3819025
rs3819025
IL17A
0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.010 1.000 1 2015 2015
dbSNP: rs3819025
rs3819025
IL17A
0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02
CUI: C0006309
Disease: Brucellosis
Brucellosis 		0.010 1.000 1 2019 2019
dbSNP: rs3819025
rs3819025
IL17A
0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02
CUI: C0852949
Disease: Arteriopathic disease
Arteriopathic disease 		0.010 1.000 1 2017 2017
dbSNP: rs3819025
rs3819025
IL17A
0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02
CUI: C0027697
Disease: Nephritis
Nephritis 		0.010 1.000 1 2016 2016
dbSNP: rs3819025
rs3819025
IL17A
0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2015 2015
dbSNP: rs3819025
rs3819025
IL17A
0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2015 2015
dbSNP: rs8193038
rs8193038
IL17A
0.925 0.080 6 52186584 intron variant A/G snv 2.2E-02
CUI: C0006309
Disease: Brucellosis
Brucellosis 		0.010 1.000 1 2013 2013
dbSNP: rs8193038
rs8193038
IL17A
0.925 0.080 6 52186584 intron variant A/G snv 2.2E-02
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.010 1.000 1 2013 2013
dbSNP: rs148704956
rs148704956
IL17A
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 		0.040 1.000 4 2010 2018
dbSNP: rs148704956
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.040 1.000 4 2010 2018
dbSNP: rs148704956
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.040 1.000 4 2014 2018