Variant (rsID / SNP)

rs267608153

rs267608153 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PMS2. Location: chromosome 7, position 6,035,165. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

PMS2Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 7:6035165
Cytoband: 7p22.1
HGVS: NM_000535.7(PMS2):c.903G>T (p.Lys301Asn)
Allele change: Missense_K110N

Associated conditions / phenotypes

Lynch syndrome|Hereditary cancer-predisposing syndrome|Hereditary nonpolyposis colorectal neoplasms|Colorectal cancer, hereditary nonpolyposis, type 4|Lynch syndrome 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.