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: rs2275913
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.050 1.000 5 2008 2014
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: rs201890924
rs201890924
IL17A
1.000 0.200 6 52187736 missense variant G/A snv 5.2E-05 2.8E-05
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.010 1.000 1 2008 2008
dbSNP: rs8193036
rs8193036
IL17A
0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72
CUI: C0004096
Disease: Asthma
Asthma 		0.020 1.000 2 2009 2016
dbSNP: rs2275913
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0004096
Disease: Asthma
Asthma 		0.060 1.000 6 2010 2018
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: 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: C0264408
Disease: Childhood asthma
Childhood asthma 		0.020 1.000 2 2010 2018
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: 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: C0376545
Disease: Hematologic Neoplasms
Hematologic Neoplasms 		0.010 1.000 1 2011 2011
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: 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: C0876973
Disease: Infectious Lung Disorder
Infectious Lung Disorder 		0.010 1.000 1 2011 2011
dbSNP: rs2275913
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0856825
Disease: Acute GVH disease
Acute GVH disease 		0.010 1.000 1 2011 2011
dbSNP: rs2275913
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.010 1.000 1 2011 2011
dbSNP: rs8193037
rs8193037
IL17A
0.752 0.320 6 52186311 upstream gene variant G/A;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 1.000 1 2011 2011
dbSNP: rs8193037
rs8193037
IL17A
0.752 0.320 6 52186311 upstream gene variant G/A;T snv
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction 		0.010 1.000 1 2011 2011
dbSNP: rs8193037
rs8193037
IL17A
0.752 0.320 6 52186311 upstream gene variant G/A;T snv
CUI: C0340293
Disease: Anterior myocardial infarction
Anterior myocardial infarction 		0.010 1.000 1 2011 2011
dbSNP: rs2275913
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.100 0.857 14 2012 2018
dbSNP: rs2275913
rs2275913
IL17A
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 		0.100 0.857 14 2012 2018
dbSNP: rs3748067
rs3748067
IL17A
0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.080 0.750 8 2012 2018
dbSNP: rs3748067
rs3748067
IL17A
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 		0.080 0.750 8 2012 2018