Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs180985111

MET

rs180985111 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MET. Location: chromosome 7, position 116,339,209. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

METConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
7:116339209
Cytoband
7q31.2
HGVS
NM_000245.4(MET):c.71G>A (p.Gly24Glu)
Allele change
Silent

Associated conditions / phenotypes

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

Public references

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