rs192966556, WNT3A

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 1 228022684 missense variant C/T snv 8.0E-06 0.010 1.000 1 2014 2014