rs111231532, TTC21A

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 3 39135911 intron variant C/T snv 5.0E-02 0.700 1.000 1 2015 2015