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.
Reasoning
CUI: C0684328
Disease: Reasoning
13 22 42146869 intron variant A/G;T snv 0.700 1.000 1 2016 2016