rs886041251, TP63

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.
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3
CUI: C1858562
Disease: ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3
14 0.882 0.360 3 189868614 missense variant C/T snv 0.700 1.000 4 1999 2003
Congenital duodenal obstruction due to malrotation of intestine
CUI: C0266184
Disease: Congenital duodenal obstruction due to malrotation of intestine
1 0.882 0.360 3 189868614 missense variant C/T snv 0.010 1.000 1 2017 2017
Lacrimoauriculodentodigital syndrome
CUI: C0265269
Disease: Lacrimoauriculodentodigital syndrome
33 0.882 0.360 3 189868614 missense variant C/T snv 0.010 1.000 1 2017 2017