Variant (rsID / SNP)

rs587782788

rs587782788 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTEN. Location: chromosome 10, position 89,725,040. Clinical significance in the table: Uncertain significance.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PTENUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 10:89725040
Cytoband: 10q23.31
HGVS: NM_000314.8(PTEN):c.1027-4C>G
Allele change: Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|PTEN hamartoma tumor 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.