rs104893829, VHL

N. diseases: 4
Disease: Renal Cell Carcinoma ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
0.010 GeneticVariation BEFREE The VHL p.P81S mutation is most likely a low-penetrant pathogenic variant predisposing to RCC development. 28503092 2017