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: rs6596
rs6596
SNX20
1.000 0.040 16 50675812 missense variant G/A;C snv 0.11; 8.0E-06
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2007 2016
dbSNP: rs2066848
rs2066848
SNX20
1.000 0.040 16 50681274 5 prime UTR variant G/A snv 0.34
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2007 2007