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Variant (rsID / SNP)

rs61762969

XRCC2

rs61762969 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to XRCC2. Location: chromosome 7, position 152,345,950. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

XRCC2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
7:152345950
Cytoband
7q36.1
HGVS
NM_005431.2(XRCC2):c.620A>G (p.Glu207Gly)
Allele change
Missense_E207G

Associated conditions / phenotypes

Colon cancer|Hereditary cancer-predisposing syndrome|Fanconi anemia complementation group U

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.