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Variant (rsID / SNP)

rs786202098

PMS2

rs786202098 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PMS2. Location: chromosome 7, position 6,042,269. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

PMS2Pathogenic
Clinical significance (as recorded)
Pathogenic/Likely pathogenic
Variant type
single nucleotide variant
Chromosome / position
7:6042269
Cytoband
7p22.1
HGVS
NM_000535.7(PMS2):c.354-2A>G
Allele change
Silent

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.