rs61758433, DNMT3B

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 20 32787389 missense variant G/A;C;T snv 8.0E-06; 2.0E-05; 7.2E-05 0.010 1.000 1 2014 2014