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: 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: rs1327295035
rs1327295035
IL17A
1.000 0.200 6 52187730 missense variant A/G snv
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.010 1.000 1 2008 2008
dbSNP: rs1360218267
rs1360218267
IL17A
1.000 0.080 6 52187734 synonymous variant C/T snv 4.0E-06
CUI: C0004096
Disease: Asthma
Asthma 		0.010 1.000 1 2011 2011
dbSNP: rs148704956
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma 		0.010 1.000 1 2014 2014
dbSNP: rs148704956
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.010 1.000 1 2014 2014
dbSNP: rs148704956
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.010 1.000 1 2019 2019
dbSNP: rs148704956
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06
CUI: C0206139
Disease: Lichen Planus, Oral
Lichen Planus, Oral 		0.010 1.000 1 2018 2018
dbSNP: rs148704956
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06
CUI: C0007107
Disease: Malignant neoplasm of larynx
Malignant neoplasm of larynx 		0.010 1.000 1 2017 2017
dbSNP: rs148704956
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06
CUI: C0031099
Disease: Periodontitis
Periodontitis 		0.010 1.000 1 2015 2015
dbSNP: rs148704956
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2014 2014
dbSNP: rs148704956
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06
CUI: C0595989
Disease: Carcinoma of larynx
Carcinoma of larynx 		0.010 1.000 1 2017 2017
dbSNP: rs148704956
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.010 1.000 1 2014 2014
dbSNP: rs148704956
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06
CUI: C0376545
Disease: Hematologic Neoplasms
Hematologic Neoplasms 		0.010 1.000 1 2011 2011
dbSNP: rs148704956
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.010 1.000 1 2015 2015
dbSNP: rs148704956
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06
CUI: C0023343
Disease: Leprosy
Leprosy 		0.010 1.000 1 2019 2019
dbSNP: rs17878530
rs17878530
IL17A
1.000 0.080 6 52189247 synonymous variant C/A;T snv 4.0E-06; 8.4E-05
CUI: C0004096
Disease: Asthma
Asthma 		0.010 1.000 1 2011 2011
dbSNP: rs17880588
rs17880588
IL17A
1.000 0.080 6 52189226 synonymous variant G/A snv 4.5E-03 1.8E-02
CUI: C0004096
Disease: Asthma
Asthma 		0.010 1.000 1 2011 2011
dbSNP: rs1974226
rs1974226
IL17A
0.827 0.240 6 52190537 3 prime UTR variant C/T snv 0.15
CUI: C0004096
Disease: Asthma
Asthma 		0.010 1.000 1 2019 2019
dbSNP: rs1974226
rs1974226
IL17A
0.827 0.240 6 52190537 3 prime UTR variant C/T snv 0.15
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2016 2016
dbSNP: rs1974226
rs1974226
IL17A
0.827 0.240 6 52190537 3 prime UTR variant C/T snv 0.15
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.010 1.000 1 2016 2016
dbSNP: rs1974226
rs1974226
IL17A
0.827 0.240 6 52190537 3 prime UTR variant C/T snv 0.15
CUI: C1719672
Disease: Severe Sepsis
Severe Sepsis 		0.010 1.000 1 2011 2011
dbSNP: rs1974226
rs1974226
IL17A
0.827 0.240 6 52190537 3 prime UTR variant C/T snv 0.15
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2016 2016