rs2742234, RET

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 10 43117161 intron variant C/T snv 0.77 0.800 1.000 1 2009 2009
Congenital Intestinal Aganglionosis
CUI: C3661523
Disease: Congenital Intestinal Aganglionosis
16 0.925 0.080 10 43117161 intron variant C/T snv 0.77 0.700 1.000 1 2009 2009