rs1157659, None

N. diseases: 2
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.
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 1.000 0.040 11 27736075 intron variant A/G snv 0.37 0.010 1.000 1 2013 2013
Mental deterioration
CUI: C0234985
Disease: Mental deterioration
121 1.000 0.040 11 27736075 intron variant A/G snv 0.37 0.010 1.000 1 2013 2013