Variant (rsID / SNP)

rs746930141

rs746930141 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTEN. Location: chromosome 10, position 89,720,768. 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: 10:89720768
Cytoband: 10q23.31
HGVS: NM_000314.8(PTEN):c.919G>C (p.Glu307Gln)
Allele change: Nonsense_E480X

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.