rs878960, GABRB3

N. diseases: 2
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.
Asperger Syndrome
CUI: C0236792
Disease: Asperger Syndrome
3 0.925 0.040 15 26683789 intron variant C/G;T snv 0.010 1.000 1 2011 2011
High-functioning autism
CUI: C3840214
Disease: High-functioning autism
5 0.925 0.040 15 26683789 intron variant C/G;T snv 0.010 1.000 1 2011 2011