RS121913243 MET

Health Risk Chr 7:116777409 snv missense variant
Upload your DNA to see your genotype for this variant.
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
Population Frequencies
gnomAD ALL
0%
Other Variants in MET
rs121913668 rs121913669 rs121913670 rs121913671 rs121913246 rs121913676 rs121913677 rs200690492 rs201154533 rs199761604
Ask Dr. Hemsworth about this variant