Source: GWASDB

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: rs2241880
rs2241880
ATG16L1 ; SCARNA5
0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.900 0.961 4 2007 2020
dbSNP: rs10210302
rs10210302
ATG16L1
1.000 0.040 2 233250193 intron variant C/A;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.810 1.000 1 2007 2010
dbSNP: rs3792109
rs3792109
ATG16L1 ; SCARNA5
1.000 0.040 2 233275771 non coding transcript exon variant G/A snv 0.45 0.42
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 2 2010 2013
dbSNP: rs12994997
rs12994997
ATG16L1
1.000 0.040 2 233264857 intron variant G/A;C snv 0.45; 4.0E-06
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2012 2012
dbSNP: rs3828309
rs3828309
ATG16L1
0.882 0.160 2 233271764 intron variant A/G snv 0.42
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2008 2008