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Variant (rsID / SNP)

rs886037859

STK11

rs886037859 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STK11. Location: chromosome 19, position 1,220,449. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

STK11Pathogenic
Clinical significance (as recorded)
Pathogenic/Likely pathogenic
Variant type
single nucleotide variant
Chromosome / position
19:1220449
Cytoband
19p13.3
HGVS
NM_000455.5(STK11):c.542A>G (p.Asn181Ser)
Allele change
Missense_N181S

Associated conditions / phenotypes

Peutz-Jeghers syndrome|Hereditary cancer-predisposing syndrome

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.