rs771174392, DNMT3A

N. diseases: 3
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.
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.925 0.200 2 25235779 missense variant T/C snv 0.700 0
Tatton Brown Rahman syndrome
CUI: C4014545
Disease: Tatton Brown Rahman syndrome
28 0.925 0.200 2 25235779 missense variant T/C snv 0.700 0
Neural Tube Defects
CUI: C0027794
Disease: Neural Tube Defects
122 0.925 0.200 2 25235779 missense variant T/C snv 0.010 1.000 1 2012 2012