Variant (rsID / SNP)

rs786204906

rs786204906 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTEN. Location: chromosome 10, position 89,720,777. Clinical significance in the table: Pathogenic.

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Reference-table entries

PTENPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Insertion
Chromosome / position: 10:89720777
Cytoband: 10q23.31
HGVS: NM_000314.8(PTEN):c.928_929insGTGCA (p.Asp310fs)

Associated conditions / phenotypes

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.