RS56391007 MET
Upload your DNA to see your genotype for this variant.
Associated Conditions
Papillary renal cell carcinoma type 1
Hereditary cancer-predisposing syndrome
Congenital diaphragmatic hernia
Renal cell carcinoma
Classic Hodgkin lymphoma
MET-related disorder
Arthrogryposis
distal
IIa 11
Autosomal recessive nonsyndromic hearing loss 97
Osteofibrous dysplasia
Hepatocellular carcinoma
Papillary renal cell carcinoma type 1
Hereditary cancer-predisposing syndrome
Congenital diaphragmatic hernia
Other Variants in MET