rs10206961, VAMP5

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 2 85587861 intron variant C/T snv 0.53 0.020 1.000 2 2016 2018
Aganglionosis, Colonic
CUI: C0085758
Disease: Aganglionosis, Colonic
11 0.925 0.080 2 85587861 intron variant C/T snv 0.53 0.010 1.000 1 2016 2016