Variant (rsID / SNP)

rs180805457

rs180805457 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to XRCC2. Location: chromosome 7, position 152,345,990. Clinical significance in the table: Uncertain significance.

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Reference-table entries

XRCC2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 7:152345990
Cytoband: 7q36.1
HGVS: NM_005431.2(XRCC2):c.580A>G (p.Thr194Ala)
Allele change: Missense_T194A

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome

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.