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: rs4077515
rs4077515
0.763 0.360 9 136372044 missense variant C/A;T snv 4.0E-06; 0.41
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.800 1.000 1 2010 2010
dbSNP: rs10870077
rs10870077
0.827 0.120 9 136369439 intron variant C/G snv 0.38
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.710 1.000 2 2008 2016
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
Digestive System Diseases 0.700 1.000 2 2015 2017
dbSNP: rs11145763
rs11145763
0.724 0.240 9 136369144 intron variant A/C;G;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs141992399
rs141992399
0.827 0.120 9 136365140 splice donor variant C/G;T snv 3.3E-03; 4.0E-06
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.700 1.000 1 2016 2016