rs6596, SNX20

N. diseases: 2
Source: GWASCAT ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
616 1.000 0.040 16 50675812 missense variant G/A;C snv 0.11; 8.0E-06 0.800 1.000 1 2007 2016
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
354 1.000 0.040 16 50675812 missense variant G/A;C snv 0.11; 8.0E-06 0.700 1.000 1 2016 2016