Variant (rsID / SNP)

rs33917957

rs33917957 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MET. Location: chromosome 7, position 116,340,262. Clinical significance in the table: Benign.

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Reference-table entries

METBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:116340262
Cytoband: 7q31.2
HGVS: NM_000245.4(MET):c.1124A>G (p.Asn375Ser)
Allele change: Silent

Associated conditions / phenotypes

Renal cell carcinoma, papillary, 1|Hereditary cancer-predisposing syndrome|Renal cell carcinoma

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.