rs7835688, NRG1

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.
Hirschsprung Disease
CUI: C0019569
Disease: Hirschsprung Disease
162 0.925 0.080 8 32553981 intron variant G/A;C;T snv 0.050 0.800 5 2014 2019
Aganglionosis, Colonic
CUI: C0085758
Disease: Aganglionosis, Colonic
11 0.925 0.080 8 32553981 intron variant G/A;C;T snv 0.010 1.000 1 2017 2017