Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs56391007
rs56391007
MET
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.720 GeneticVariation BEFREE A selective effect of MET-T1010I as compared to wild type MET on cell invasion both in-vitro and in-vivo suggests that the MET-T1010I SNP may alter tumor pathophysiology and should be considered as a potential biomarker when implementing MET targeted clinical trials. 25605252

2015

dbSNP: rs56391007
rs56391007
MET
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.720 GeneticVariation BEFREE These include two different c-MET missense mutations in the juxtamembrane (JM) domain (R988C found in NCI-H69 and H249 cell lines; and T1010I in SCLC tumor sample T31). 14559814

2003