Variant (rsID / SNP)

rs146848345

rs146848345 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PMS2. Location: chromosome 7, position 6,026,958. Clinical significance in the table: Uncertain significance.

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Reference-table entries

PMS2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 7:6026958
Cytoband: 7p22.1
HGVS: NM_000535.7(PMS2):c.1438G>C (p.Gly480Arg)
Allele change: Missense_G289R

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|BAP1-related tumor predisposition 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.