Variant (rsID / SNP)

rs267608159

rs267608159 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PMS2. Location: chromosome 7, position 6,027,157. Clinical significance in the table: Pathogenic.

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Reference-table entries

PMS2Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Deletion
Chromosome / position: 7:6027157
Cytoband: 7p22.1
HGVS: NM_000535.7(PMS2):c.1237_1239del (p.Lys413del)

Associated conditions / phenotypes

Colorectal cancer, hereditary nonpolyposis, type 4

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.