Variant (rsID / SNP)

rs121913316

rs121913316 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STK11. Location: chromosome 19, position 1,220,488. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

STK11Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 19:1220488
Cytoband: 19p13.3
HGVS: NM_000455.5(STK11):c.581A>T (p.Asp194Val)
Allele change: Missense_D194V

Associated conditions / phenotypes

Neoplasm

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.