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Variant (rsID / SNP)

rs201687037

MET

rs201687037 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MET. Location: chromosome 7, position 116,340,039. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

METConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
7:116340039
Cytoband
7q31.2
HGVS
NM_000245.4(MET):c.901A>G (p.Thr301Ala)
Allele change
Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Renal cell carcinoma|Autosomal recessive nonsyndromic hearing loss 97

Public references

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