[PMID 20416453] c-MET pathway involvement in chronic rhinosinusitis: a genetic association analysis

[PMID 19002214] MET and autism susceptibility: family and case-control studies.

[PMID 20011629] The hepatocyte growth factor receptor (MET) gene is not associated with refractive error and ocular biometrics in a Caucasian population.

[PMID 20080979] Association of genetic variation in the MET proto-oncogene with schizophrenia and general cognitive ability.


[PMID 24766640] Evaluation of MYOC, ACAN, HGF, and MET as Candidate Genes for High Myopia in a Han Chinese Population

rs38857

Parent Gene: MET

Importance: 1
Less common allele: T = 22%
More common allele: C = 78%
My Genotype: Log In