Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893829
rs104893829
VHL
CUI: C0007134
Disease: Renal Cell Carcinoma
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