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Variant (rsID / SNP)

rs786201280

PTEN

rs786201280 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTEN. Location: chromosome 10, position 89,624,304. Clinical significance in the table: Uncertain significance.

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Reference-table entries

PTENUncertain significance
Clinical significance (as recorded)
Uncertain significance
Variant type
single nucleotide variant
Chromosome / position
10:89624304
Cytoband
10q23.31
HGVS
NM_000314.8(PTEN):c.78C>T (p.Thr26=)
Allele change
Synonymous_T199T

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|PTEN hamartoma tumor syndrome|Cowden syndrome 1

Public references

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