rs121908840, TP63

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.
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3
CUI: C1858562
Disease: ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3
14 0.925 0.160 3 189867903 missense variant G/A snv 0.800 1.000 4 1999 2003
RAPP-HODGKIN SYNDROME
CUI: C1785148
Disease: RAPP-HODGKIN SYNDROME
3 0.925 0.160 3 189867903 missense variant G/A snv 0.800 1.000 3 2003 2004