rs137854573, APC

N. diseases: 10
Disease: Hepatoblastoma ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hepatoblastoma
CUI: C0206624
Disease: Hepatoblastoma
0.010 GeneticVariation BEFREE The mutation of APC (rs137854573, c.C1606T, p.R536X) could result in HB carcinogenesis by activating Wnt signaling. 30619485 2018