RS56391007 MET

Health Risk Chr 7:116771935 snv missense variant
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
Population Frequencies
gnomAD ALL
1.1%
1kG AFR
100%
1kG ALL
99.7%
1kG AMR
99.4%
1kG EAS
100%
1kG EUR
98.8%
1kG SAS
0.1%
Other Variants in MET
rs121913668 rs121913669 rs121913670 rs121913671 rs121913246 rs121913243 rs121913676 rs121913677 rs200690492 rs201154533
Ask Dr. Hemsworth about this variant