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Variant (rsID / SNP)

rs532889728

STK11

rs532889728 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STK11. Location: chromosome 19, position 1,220,597. 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
19:1220597
Cytoband
19p13.3
HGVS
NM_000455.5(STK11):c.615G>A (p.Ala205=)
Allele change
Synonymous_A205A

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Peutz-Jeghers syndrome|Hereditary breast ovarian cancer syndrome

Public references

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