Variant (rsID / SNP)

rs137853078

rs137853078 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STK11. Location: chromosome 19, position 1,220,395. 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: 19:1220395
Cytoband: 19p13.3
HGVS: NM_000455.5(STK11):c.488G>A (p.Gly163Asp)
Allele change: Missense_G163D

Associated conditions / phenotypes

Malignant tumor of testis|Hereditary cancer-predisposing 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.