rs11795613, NLGN3

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.
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.925 0.120 X 71147478 intron variant A/G snv 0.010 1.000 1 2011 2011
Hirschsprung Disease
CUI: C0019569
Disease: Hirschsprung Disease
162 0.925 0.120 X 71147478 intron variant A/G snv 0.010 1.000 1 2018 2018