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 1 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 1 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 3 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 5 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 1 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 2 2007 2014
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 1 2007 2017
dbSNP: rs72796367
rs72796367
0.827 0.120 16 50728860 intron variant T/C snv 1.9E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.700 1.000 1 2016 2016