Variant (rsID / SNP)

rs573125799

rs573125799 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PMS2. Location: chromosome 7, position 6,036,995. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

PMS2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 7:6036995
Cytoband: 7p22.1
HGVS: NM_000535.7(PMS2):c.765C>T (p.Tyr255=)
Allele change: Nonsense_Y64X

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Hereditary nonpolyposis colorectal neoplasms

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.