rs141893504, SEMA3D

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 7 85022533 missense variant G/T snv 4.0E-03 4.2E-03 0.700 0