Disease: Crohn Disease ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2066844
rs2066844 		0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 1.000 0.940 83 2001 2018
dbSNP: rs2066845
rs2066845 		0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 1.000 0.949 78 2001 2019
dbSNP: rs2066847
rs2066847 		0.716 0.400 16 50729868 frameshift variant C/-;CC delins 1.5E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.890 0.923 13 2005 2019
dbSNP: rs2076756
rs2076756 		0.882 0.040 16 50722970 intron variant A/G snv 0.17
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.830 1.000 9 2007 2019
dbSNP: rs5743293
rs5743293 		0.807 0.200 16 50729868 frameshift variant C/-;CC delins
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.830 1.000 8 2007 2017
dbSNP: rs17221417
rs17221417 		0.925 0.040 16 50705671 intron variant C/G snv 0.20
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.810 1.000 3 2007 2017
dbSNP: rs5743289
rs5743289 		1.000 0.040 16 50722863 intron variant C/G;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.810 1.000 3 2007 2014
dbSNP: rs2066842
rs2066842 		0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.790 1.000 10 2002 2014
dbSNP: rs104895467
rs104895467 		0.851 0.120 16 50716899 missense variant A/G snv 1.2E-03 7.5E-04
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.720 < 0.001 2 2014 2018
dbSNP: rs5743272
rs5743272 		1.000 0.040 16 50710966 missense variant A/G snv 9.6E-04 3.8E-03
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.710 1.000 7 2001 2018
dbSNP: rs5743277
rs5743277 		1.000 0.040 16 50712018 missense variant C/G;T snv 1.2E-05; 3.2E-03
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.710 1.000 7 2001 2016
dbSNP: rs17313265
rs17313265 		1.000 0.040 16 50713793 intron variant C/T snv 0.20
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.710 1.000 2 2007 2014
dbSNP: rs2066843
rs2066843 		0.925 0.040 16 50711288 synonymous variant C/A;T snv 0.19
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.710 1.000 2 2006 2010
dbSNP: rs5743291
rs5743291 		0.925 0.040 16 50723365 missense variant G/A snv 6.3E-02 6.0E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.710 1.000 2 2007 2008
dbSNP: rs104895483
rs104895483 		1.000 0.040 16 50712049 missense variant G/A snv 4.7E-04 5.4E-04
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.710 1.000 1 2006 2006
dbSNP: rs3813758
rs3813758 		1.000 0.040 16 50712189 missense variant C/T snv 2.0E-05 1.4E-05
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.710 1.000 1 2006 2006
dbSNP: rs62029861
rs62029861 		1.000 0.040 16 50712279 missense variant C/T snv 8.4E-05 4.9E-05
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.710 1.000 1 2006 2006
dbSNP: rs104895420
rs104895420 		1.000 0.040 16 50699883 missense variant T/C snv 1.3E-04 5.6E-05
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 6 2001 2016
dbSNP: rs104895422
rs104895422 		1.000 0.040 16 50710614 missense variant C/T snv 1.0E-04 1.3E-04
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 6 2001 2016
dbSNP: rs104895423
rs104895423 		1.000 0.040 16 50710654 missense variant T/G snv 5.6E-04 2.6E-04
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 6 2001 2016
dbSNP: rs104895424
rs104895424 		1.000 0.040 16 50710782 missense variant G/A snv 8.0E-06 2.1E-05
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 6 2001 2016
dbSNP: rs104895425
rs104895425 		1.000 0.040 16 50710792 missense variant C/G snv 1.9E-03 1.5E-03
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 6 2001 2016
dbSNP: rs104895426
rs104895426 		1.000 0.040 16 50710813 missense variant C/T snv 4.4E-05 4.2E-05
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 6 2001 2016
dbSNP: rs104895427
rs104895427 		1.000 0.040 16 50710842 missense variant C/A;T snv 5.9E-04
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 6 2001 2016
dbSNP: rs145293873
rs145293873 		1.000 0.040 16 50711028 missense variant C/T snv 1.8E-04 2.1E-04
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 6 2001 2016