rs1800764, None

N. diseases: 10
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 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 0.020 1.000 2 2014 2014