Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786202529
rs786202529
PTEN
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		AG 0.700 CausalMutation CLINVAR Different splicing defects lead to differential effects downstream of the lipid and protein phosphatase activities of PTEN. 16014636

2005