Source: GWASCAT

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: rs2076756
rs2076756
0.882 0.040 16 50722970 intron variant A/G snv 0.17
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.830 1.000 5 2007 2019
dbSNP: rs11742570
rs11742570
0.925 0.040 5 40410482 upstream gene variant T/C;G snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 4 2010 2017
dbSNP: rs4409764
rs4409764
0.925 0.040 10 99524480 upstream gene variant T/A;G snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.820 1.000 4 2010 2019
dbSNP: rs10495903
rs10495903
1.000 0.040 2 43579779 intron variant C/T snv 0.13
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 3 2010 2017
dbSNP: rs10761659
rs10761659
0.925 0.040 10 62685804 intron variant A/G snv 0.43
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.810 1.000 3 2010 2017
dbSNP: rs2413583
rs2413583
0.925 0.040 22 39263768 intron variant C/T snv 0.19
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 3 2010 2017
dbSNP: rs7554511
rs7554511
0.925 0.040 1 200908434 intron variant C/A snv 0.22
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 3 2010 2017
dbSNP: rs1042058
rs1042058
1.000 0.040 10 30439172 synonymous variant T/C snv 0.51 0.45
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.710 1.000 2 2015 2017
dbSNP: rs10486483
rs10486483
1.000 0.040 7 26852821 intron variant G/A snv 0.21
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 2 2012 2015
dbSNP: rs10781499
rs10781499
0.925 0.040 9 136371953 synonymous variant G/A snv 0.41 0.38
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 2 2015 2017
dbSNP: rs11195128
rs11195128
1.000 0.040 10 110426390 downstream gene variant C/G;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.810 1.000 2 2014 2017
dbSNP: rs11681525
rs11681525
1.000 0.040 2 144734815 intron variant C/G snv 5.9E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 2 2015 2017
dbSNP: rs11741861
rs11741861
0.925 0.040 5 150898347 intron variant A/G snv 8.8E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 2 2015 2017
dbSNP: rs11879191
rs11879191
1.000 0.040 19 10402235 intron variant G/A;C snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 2 2015 2017
dbSNP: rs1292053
rs1292053
1.000 0.040 17 59886176 missense variant A/G snv 0.45 0.46
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 2 2015 2017
dbSNP: rs13126505
rs13126505
1.000 0.040 4 101944147 intron variant G/A snv 4.1E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 2 2012 2017
dbSNP: rs1363907
rs1363907
1.000 0.040 5 96917099 intron variant G/A snv 0.38
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 2 2015 2017
dbSNP: rs17694108
rs17694108
0.925 0.040 19 33240645 regulatory region variant G/A snv 0.22
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 2 2015 2017
dbSNP: rs1819333
rs1819333
1.000 0.040 6 166960059 upstream gene variant T/G snv 0.57
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 2 2015 2017
dbSNP: rs1819658
rs1819658
1.000 0.040 10 58153390 regulatory region variant C/G;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 2 2010 2017
dbSNP: rs2062305
rs2062305
1.000 0.040 13 42478744 intron variant G/A snv 0.46
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 2 2010 2017
dbSNP: rs2823286
rs2823286
0.925 0.040 21 15445619 intron variant G/A snv 0.28
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 2 2015 2017
dbSNP: rs2930047
rs2930047
DAP
0.925 0.040 5 10695414 intron variant T/C snv 0.49
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 2 2015 2017
dbSNP: rs2945412
rs2945412
1.000 0.040 17 27516617 intron variant G/A snv 0.65
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 2 2012 2015
dbSNP: rs3091315
rs3091315
1.000 0.040 17 34266646 upstream gene variant A/G snv 0.33
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 2 2010 2015