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: rs1020856343
rs1020856343
SLC22A5
0.851 0.240 5 132393705 missense variant C/T snv 4.0E-06
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.050 0.800 5 2006 2012
dbSNP: rs2631367
rs2631367
SLC22A5 ; MIR3936HG
0.925 0.120 5 132369766 5 prime UTR variant C/G snv 0.59
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 1.000 1 2011 2011
dbSNP: rs2631372
rs2631372
SLC22A5 ; MIR3936HG
1.000 0.040 5 132367886 intron variant G/C snv 0.29
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 1.000 1 2011 2011