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: 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
dbSNP: rs3828309
rs3828309
ATG16L1
0.882 0.160 2 233271764 intron variant A/G snv 0.42
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2011 2011
dbSNP: rs3828309
rs3828309
ATG16L1
0.882 0.160 2 233271764 intron variant A/G snv 0.42
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2011 2011