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: 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: rs8193036
rs8193036
IL17A
0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.010 1.000 1 2012 2012
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: C2936258
Disease: Peri-Implantitis
Peri-Implantitis 		0.010 1.000 1 2013 2013
dbSNP: rs2275913
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		0.010 1.000 1 2013 2013
dbSNP: rs2275913
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0031090
Disease: Periodontal Diseases
Periodontal Diseases 		0.010 1.000 1 2013 2013
dbSNP: rs2275913
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
Malignant neoplasm of urinary bladder 		0.010 1.000 1 2013 2013
dbSNP: rs2275913
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm 		0.010 1.000 1 2013 2013
dbSNP: rs2275913
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0409980
Disease: Primary antiphospholipid syndrome
Primary antiphospholipid syndrome 		0.010 1.000 1 2013 2013
dbSNP: rs2275913
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.010 1.000 1 2013 2013
dbSNP: rs2275913
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder 		0.010 1.000 1 2013 2013
dbSNP: rs2275913
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.010 1.000 1 2013 2013
dbSNP: rs2275913
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic 		0.010 < 0.001 1 2013 2013
dbSNP: rs2275913
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2013 2013
dbSNP: rs3748067
rs3748067
IL17A
0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-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: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.010 1.000 1 2013 2013
dbSNP: rs8193036
rs8193036
IL17A
0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.010 1.000 1 2013 2013
dbSNP: rs8193036
rs8193036
IL17A
0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		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: 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: 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: 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: 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: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.010 1.000 1 2014 2014