rs6439886, CLSTN2

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 139963653 intron variant A/G snv 0.14 0.010 1.000 1 2012 2012