rs6651252, LINC00824

N. diseases: 1
Source: GWASDB ×
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
332 0.790 0.200 8 128554935 intron variant T/C snv 0.19 0.810 1.000 2 2010 2019