Variant (rsID / SNP)

rs1057520018

rs1057520018 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STK11. Location: chromosome 19, position 1,223,123. 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: single nucleotide variant
Chromosome / position: 19:1223123
Cytoband: 19p13.3
HGVS: NM_000455.5(STK11):c.1060T>C (p.Phe354Leu)
Allele change: Missense_F354L

Associated conditions / phenotypes

Squamous cell lung carcinoma|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.