Source: ALL

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: rs11190140
rs11190140
NKX2-3 ; LINC01475
0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.810 1.000 2 2008 2014
dbSNP: rs11190141
rs11190141
NKX2-3 ; LINC01475
1.000 0.040 10 99532633 upstream gene variant C/T snv 0.40
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2012 2012
dbSNP: rs888208
rs888208
NKX2-3
0.882 0.080 10 99536106 3 prime UTR variant A/G snv 0.25
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 1.000 1 2011 2011