Variant (rsID / SNP)

rs137853081

rs137853081 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STK11. Location: chromosome 19, position 1,219,351. Clinical significance in the table: Pathogenic.

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Reference-table entries

STK11Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 19:1219351
Cytoband: 19p13.3
HGVS: NM_000455.5(STK11):c.403G>C (p.Gly135Arg)
Allele change: Missense_G135R

Associated conditions / phenotypes

Melanoma, cutaneous malignant, susceptibility to, 1

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.