rs17706989, WWOX

N. diseases: 1
Source: ALL
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.
Reasoning
CUI: C0684328
Disease: Reasoning
13 16 78536060 intron variant C/G snv 2.6E-02 0.700 1.000 1 2011 2011