Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908845
rs121908845
TP63
0.710 GeneticVariation BEFREE In addition, we evaluated the conformation and the interaction with Itch-WW2 of a site specific mutant of p63, I549T, that has been reported in both Hay-Wells syndrome and Rapp-Hodgkin syndrome. 20855944

2010
dbSNP: rs121908845
rs121908845
TP63
C 0.710 CausalMutation CLINVAR