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: rs10852936
rs10852936
0.925 0.120 17 39875461 intron variant C/T snv 0.39 0.40
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.010 1.000 1 2014 2014
dbSNP: rs11557467
rs11557467
0.851 0.200 17 39872381 missense variant G/T snv 0.45 0.45
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.010 1.000 1 2013 2013
dbSNP: rs12150079
rs12150079
0.807 0.280 17 39869164 intron variant G/A snv 0.24
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.010 1.000 1 2018 2018
dbSNP: rs12150079
rs12150079
0.807 0.280 17 39869164 intron variant G/A snv 0.24
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2018 2018
dbSNP: rs12150079
rs12150079
0.807 0.280 17 39869164 intron variant G/A snv 0.24
CUI: C0014378
Disease: Enterovirus Infections
Enterovirus Infections
0.010 1.000 1 2015 2015
dbSNP: rs12150079
rs12150079
0.807 0.280 17 39869164 intron variant G/A snv 0.24
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs12150079
rs12150079
0.807 0.280 17 39869164 intron variant G/A snv 0.24
Diabetes Mellitus, Insulin-Dependent
0.010 1.000 1 2015 2015
dbSNP: rs12150079
rs12150079
0.807 0.280 17 39869164 intron variant G/A snv 0.24
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.010 1.000 1 2018 2018
dbSNP: rs12150079
rs12150079
0.807 0.280 17 39869164 intron variant G/A snv 0.24
CUI: C0018213
Disease: Graves Disease
Graves Disease
0.010 < 0.001 1 2018 2018
dbSNP: rs12150079
rs12150079
0.807 0.280 17 39869164 intron variant G/A snv 0.24
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2018 2018
dbSNP: rs189660050
rs189660050
1.000 0.040 17 39870781 missense variant C/T snv 2.8E-05 1.9E-04
CUI: C0740394
Disease: Hyperuricemia
Hyperuricemia
0.010 1.000 1 2011 2011
dbSNP: rs11557467
rs11557467
0.851 0.200 17 39872381 missense variant G/T snv 0.45 0.45
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 2 2012 2012
dbSNP: rs12150079
rs12150079
0.807 0.280 17 39869164 intron variant G/A snv 0.24
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 2 2010 2011
dbSNP: rs12936231
rs12936231
0.925 0.160 17 39872867 intron variant C/G;T snv
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 2 2012 2012
dbSNP: rs1054609
rs1054609
0.925 0.160 17 39877024 3 prime UTR variant A/C snv 0.40
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2011 2011
dbSNP: rs1054609
rs1054609
0.925 0.160 17 39877024 3 prime UTR variant A/C snv 0.40
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs10852935
rs10852935
1.000 0.080 17 39875421 synonymous variant C/T snv 0.40 0.35
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs10852936
rs10852936
0.925 0.120 17 39875461 intron variant C/T snv 0.39 0.40
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs10852936
rs10852936
0.925 0.120 17 39875461 intron variant C/T snv 0.39 0.40
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2013 2013
dbSNP: rs11078925
rs11078925
0.925 0.160 17 39868955 intron variant T/C snv 0.36
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2013 2013
dbSNP: rs11078925
rs11078925
0.925 0.160 17 39868955 intron variant T/C snv 0.36
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2011 2011
dbSNP: rs11078925
rs11078925
0.925 0.160 17 39868955 intron variant T/C snv 0.36
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs11557466
rs11557466
0.925 0.160 17 39868373 synonymous variant C/T snv 0.40 0.36
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2013 2013
dbSNP: rs11557466
rs11557466
0.925 0.160 17 39868373 synonymous variant C/T snv 0.40 0.36
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2011 2011
dbSNP: rs11557466
rs11557466
0.925 0.160 17 39868373 synonymous variant C/T snv 0.40 0.36
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012