Variant (rsID / SNP)

rs59912467

rs59912467 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STK11. Location: chromosome 19, position 1,223,125. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

STK11Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 19:1223125
Cytoband: 19p13.3
HGVS: NM_000455.5(STK11):c.1062C>G (p.Phe354Leu)
Allele change: Missense_F354L

Associated conditions / phenotypes

Peutz-Jeghers syndrome|Hereditary cancer-predisposing syndrome|Malignant tumor of breast|Breast and/or ovarian cancer

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.