RS121913243 MET
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What This Variant Does
"[OMIM:?]
Associated Conditions
Papillary renal cell carcinoma type 1
Renal cell carcinoma
Hereditary cancer-predisposing syndrome
MET-related disorder
Hepatocellular carcinoma
Osteofibrous dysplasia
Arthrogryposis
distal
IIa 11
Autosomal recessive nonsyndromic hearing loss 97
Papillary renal cell carcinoma type 1
Renal cell carcinoma
Hereditary cancer-predisposing syndrome
MET-related disorder
Hepatocellular carcinoma
Other Variants in MET