rs10883866, NRG3

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.
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.882 0.160 10 81883883 intron variant C/A;G;T snv 0.020 1.000 2 2010 2011
Delusions
CUI: C0011253
Disease: Delusions
15 0.882 0.160 10 81883883 intron variant C/A;G;T snv 0.010 1.000 1 2010 2010
Hirschsprung Disease
CUI: C0019569
Disease: Hirschsprung Disease
162 0.882 0.160 10 81883883 intron variant C/A;G;T snv 0.010 1.000 1 2017 2017