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: 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: rs11650661
rs11650661
1.000 0.080 17 39870033 intron variant A/C;T snv
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs4795397
rs4795397
0.925 0.160 17 39867492 upstream gene variant A/G snv 0.38
CUI: C0004096
Disease: Asthma
Asthma
0.710 1.000 2 2012 2017
dbSNP: rs12709365
rs12709365
1.000 0.080 17 39871147 intron variant A/G snv 0.40
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs13380815
rs13380815
1.000 0.080 17 39871330 intron variant A/G snv 0.40
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs4795397
rs4795397
0.925 0.160 17 39867492 upstream gene variant A/G snv 0.38
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs4795397
rs4795397
0.925 0.160 17 39867492 upstream gene variant A/G snv 0.38
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.700 1.000 1 2015 2015
dbSNP: rs4795397
rs4795397
0.925 0.160 17 39867492 upstream gene variant A/G snv 0.38
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2013 2013
dbSNP: rs12936231
rs12936231
0.925 0.160 17 39872867 intron variant C/G;T snv
CUI: C0004096
Disease: Asthma
Asthma
0.720 1.000 3 2011 2019
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: rs12936231
rs12936231
0.925 0.160 17 39872867 intron variant C/G;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2013 2013
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: C0033860
Disease: Psoriasis
Psoriasis
0.010 1.000 1 2014 2014
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: 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
dbSNP: rs11655198
rs11655198
1.000 0.080 17 39869916 intron variant C/T snv 0.43
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2016 2016
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: rs34189114
rs34189114
1.000 0.080 17 39876207 intron variant C/T snv 0.36
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 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: 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