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Variant (rsID / SNP)

rs786203510

PMS2

rs786203510 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PMS2. Location: chromosome 7, position 6,026,952. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

PMS2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
7:6026952
Cytoband
7p22.1
HGVS
NM_000535.7(PMS2):c.1444A>G (p.Ser482Gly)
Allele change
Missense_S291G

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Hereditary nonpolyposis colorectal neoplasms

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.