Variant (rsID / SNP)

rs764449808

rs764449808 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STK11. Location: chromosome 19, position 1,218,493. Clinical significance in the table: Uncertain significance.

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Reference-table entries

STK11Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 19:1218493
Cytoband: 19p13.3
HGVS: NM_000455.5(STK11):c.368A>G (p.Gln123Arg)
Allele change: Missense_Q123R

Associated conditions / phenotypes

Squamous cell lung carcinoma|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.