Variant (rsID / SNP)

rs752464256

rs752464256 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STK11. Location: chromosome 19, position 1,222,966. Clinical significance in the table: Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

STK11Likely benign

Clinical significance (as recorded): Likely benign
Variant type: Deletion
Chromosome / position: 19:1222966
Cytoband: 19p13.3
HGVS: NM_000455.5(STK11):c.921-18_921-15del

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Peutz-Jeghers 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.