Variant (rsID / SNP)

rs200690492

rs200690492 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MET. Location: chromosome 7, position 116,340,157. Clinical significance in the table: Uncertain significance.

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Reference-table entries

METUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 7:116340157
Cytoband: 7q31.2
HGVS: NM_000245.4(MET):c.1019A>G (p.Asp340Gly)
Allele change: Silent

Associated conditions / phenotypes

Renal cell carcinoma|Hereditary cancer-predisposing syndrome

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.