SNX20, sorting nexin 20, 124460

N. diseases: 4; N. variants: 3
Disease: Crohn Disease ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6596
rs6596 		1.000 0.040 16 50675812 missense variant G/A;C snv 0.11; 8.0E-06
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.800 1.000 2 2007 2016
dbSNP: rs2066848
rs2066848 		1.000 0.040 16 50681274 5 prime UTR variant G/A snv 0.34
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs2270368
rs2270368 		0.925 0.080 16 50680424 intron variant G/A;C snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.010 1.000 1 2017 2017