Variant (rsID / SNP)

rs786204929

rs786204929 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTEN. Location: chromosome 10, position 89,692,901. 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: 10:89692901
Cytoband: 10q23.31
HGVS: NM_000314.8(PTEN):c.385G>A (p.Gly129Arg)
Allele change: Missense_G302R

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Inborn genetic diseases|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.