Variant (rsID / SNP)

rs35775721

rs35775721 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MET. Location: chromosome 7, position 116,339,672. 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: 7:116339672
Cytoband: 7q31.2
HGVS: NM_000245.4(MET):c.534C>T (p.Ser178=)
Allele change: Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Renal cell carcinoma, papillary, 1|Renal cell carcinoma|Autosomal recessive nonsyndromic hearing loss 97

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.