Variant (rsID / SNP)

rs121913323

rs121913323 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STK11. Location: chromosome 19, position 1,220,415. 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: 19:1220415
Cytoband: 19p13.3
HGVS: NM_000455.5(STK11):c.508C>T (p.Gln170Ter)
Allele change: Nonsense_Q170X

Associated conditions / phenotypes

Melanoma, cutaneous malignant, susceptibility to, 1|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.