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: rs7608910
rs7608910
0.827 0.120 2 60977721 intron variant A/G snv 0.37
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2017
dbSNP: rs925255
rs925255
0.827 0.120 2 28391927 intron variant C/T snv 0.38
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2017
dbSNP: rs9297145
rs9297145
0.827 0.120 7 99161494 intergenic variant C/A snv 0.67
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2017
dbSNP: rs941823
rs941823
0.827 0.120 13 40439840 intron variant T/C snv 0.77
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2017
dbSNP: rs2836878
rs2836878
0.851 0.200 21 39093608 intergenic variant G/A snv 0.23
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 2 2008 2017
dbSNP: rs1250550
rs1250550
0.851 0.240 10 79300560 intron variant C/A snv 0.27
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.810 1.000 1 2009 2017
dbSNP: rs12946510
rs12946510
0.851 0.160 17 39756124 downstream gene variant C/T snv 0.37
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2017
dbSNP: rs1517352
rs1517352
0.851 0.160 2 191066738 intron variant A/C snv 0.45
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2015
dbSNP: rs1569723
rs1569723
0.851 0.280 20 46113425 upstream gene variant C/A snv 0.80
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2012
dbSNP: rs6871626
rs6871626
0.851 0.160 5 159399784 intron variant C/A;G snv 0.29
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.820 0.667 1 2012 2017
dbSNP: rs1456896
rs1456896
0.882 0.200 7 50264865 upstream gene variant C/T snv 0.67
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2017
dbSNP: rs17119
rs17119
0.882 0.120 6 14719265 intron variant G/A snv 0.74
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2017
dbSNP: rs2006996
rs2006996
0.882 0.080 9 114830358 regulatory region variant T/C snv 7.2E-02
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.700 1.000 1 2011 2011
dbSNP: rs2076756
rs2076756
0.882 0.040 16 50722970 intron variant A/G snv 0.17
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.820 1.000 1 2006 2017
dbSNP: rs2188962
rs2188962
0.882 0.160 5 132435113 intron variant C/T snv 0.29
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2017
dbSNP: rs7282490
rs7282490
0.882 0.080 21 44195858 intron variant G/A;T snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2017
dbSNP: rs8005161
rs8005161
0.882 0.120 14 88006251 intron variant C/T snv 0.18
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.810 1.000 1 2012 2019
dbSNP: rs907611
rs907611
0.882 0.160 11 1852842 upstream gene variant G/A snv 0.26
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2017
dbSNP: rs913678
rs913678
0.882 0.240 20 50338887 regulatory region variant T/C snv 0.51
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2017
dbSNP: rs10761659
rs10761659
0.925 0.040 10 62685804 intron variant A/G snv 0.43
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2017
dbSNP: rs10781499
rs10781499
0.925 0.040 9 136371953 synonymous variant G/A snv 0.41 0.38
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2017
dbSNP: rs11010067
rs11010067
0.925 0.040 10 35006503 downstream gene variant C/G snv 0.37
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2015
dbSNP: rs11741861
rs11741861
0.925 0.040 5 150898347 intron variant A/G snv 8.8E-02
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2017
dbSNP: rs11742570
rs11742570
0.925 0.040 5 40410482 upstream gene variant T/C;G snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2017
dbSNP: rs12103
rs12103
0.925 0.040 1 1312114 synonymous variant T/A;C;G snv 0.56
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2017