rs59197085, CCDC136

N. diseases: 3
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.
Dyslexia
CUI: C0476254
Disease: Dyslexia
30 0.925 0.120 7 128820702 intron variant G/A snv 9.9E-02 0.700 1.000 1 2014 2014
Intelligence
CUI: C0021704
Disease: Intelligence
2093 0.925 0.120 7 128820702 intron variant G/A snv 9.9E-02 0.700 1.000 1 2014 2014
Specific language impairment
CUI: C0454651
Disease: Specific language impairment
9 0.925 0.120 7 128820702 intron variant G/A snv 9.9E-02 0.700 1.000 1 2014 2014