rs117129097, None

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.
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 1.000 0.040 12 128054737 intron variant C/G;T snv 1.9E-03 0.010 1.000 1 2019 2019