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Variant (rsID / SNP)

rs786204862

PTEN

rs786204862 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTEN. Location: chromosome 10, position 89,711,874. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

PTENPathogenic
Clinical significance (as recorded)
Pathogenic/Likely pathogenic
Variant type
single nucleotide variant
Chromosome / position
10:89711874
Cytoband
10q23.31
HGVS
NM_000314.8(PTEN):c.493-1G>A
Allele change
Silent

Associated conditions / phenotypes

PTEN hamartoma tumor syndrome|Hereditary cancer-predisposing syndrome

Public references

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