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: 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: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.900 0.773 2 2006 2020
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 3 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 3 2012 2017
dbSNP: rs12942547
rs12942547
0.807 0.200 17 42375526 intron variant A/G;T snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 3 2012 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 3 2012 2017
dbSNP: rs1363907
rs1363907
1.000 0.040 5 96917099 intron variant G/A snv 0.38
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 3 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 3 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 3 2012 2017
dbSNP: rs17293632
rs17293632
0.763 0.240 15 67150258 intron variant C/T snv 0.17
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 3 2012 2017
dbSNP: rs17694108
rs17694108
0.925 0.040 19 33240645 regulatory region variant G/A snv 0.22
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 3 2012 2017
dbSNP: rs1801274
rs1801274
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 3 2012 2017
dbSNP: rs1819333
rs1819333
1.000 0.040 6 166960059 upstream gene variant T/G snv 0.57
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 3 2012 2017
dbSNP: rs1847472
rs1847472
0.807 0.200 6 90263440 intron variant C/A snv 0.25
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 3 2012 2017
dbSNP: rs259964
rs259964
0.827 0.120 20 59249254 intron variant A/G;T snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 3 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 3 2008 2017
dbSNP: rs4845604
rs4845604
0.776 0.200 1 151829204 intron variant G/A;C;T snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 3 2012 2017
dbSNP: rs6920220
rs6920220
0.742 0.440 6 137685367 intron variant G/A snv 0.16
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 3 2012 2017
dbSNP: rs7240004
rs7240004
1.000 0.040 18 48868651 intergenic variant A/G snv 0.43
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 3 2012 2017
dbSNP: rs7404095
rs7404095
0.827 0.120 16 23853269 intron variant T/C snv 0.58
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 3 2012 2017
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 3 2012 2017
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 3 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 3 2012 2017
dbSNP: rs9358372
rs9358372
1.000 0.040 6 20812357 intron variant G/A snv 0.64
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 3 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 3 2012 2017