rs17059206, FZD3

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 8 28554946 intron variant A/T snv 1.8E-02 0.010 1.000 1 2016 2016