rs11718165, BSN

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 1.000 0.040 3 49659364 intron variant A/G snv 0.27 0.700 1.000 1 2007 2007