Variant (rsID / SNP)

rs145085742

rs145085742 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to XRCC2. Location: chromosome 7, position 152,345,762. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

XRCC2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 7:152345762
Cytoband: 7q36.1
HGVS: NM_005431.2(XRCC2):c.808T>G (p.Phe270Val)
Allele change: Missense_F270V

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Fanconi anemia complementation group U

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.