rs372958987, EDN3

N. diseases: 1
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 1.000 0.080 20 59324430 missense variant C/A;G;T snv 2.0E-05; 3.6E-05 0.010 1.000 1 1998 1998