rs13223150, TSGA13

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.
Aganglionosis, Colonic
CUI: C0085758
Disease: Aganglionosis, Colonic
11 0.925 0.080 7 130684771 intron variant A/C snv 0.48 0.010 1.000 1 2019 2019
Hirschsprung Disease
CUI: C0019569
Disease: Hirschsprung Disease
162 0.925 0.080 7 130684771 intron variant A/C snv 0.48 0.010 1.000 1 2019 2019