Variant (rsID / SNP)
rs3218536
rs3218536 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to XRCC2. Location: chromosome 7, position 152,346,007. Clinical significance in the table: Benign.
Reference-table entries
XRCC2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:152346007
- Cytoband
- 7q36.1
- HGVS
- NM_005431.2(XRCC2):c.563G>A (p.Arg188His)
- Allele change
- Missense_R188H
Associated conditions / phenotypes
Hereditary cancer-predisposing syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.