rs17108533, MAP3K9

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.
Reasoning
CUI: C0684328
Disease: Reasoning
13 14 70783085 intron variant C/A;G;T snv 0.10 0.700 1.000 1 2011 2011