Variant (rsID / SNP)

rs861539

rs861539 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to XRCC3, KLC1. Location: chromosome 14, position 104,165,753. Clinical significance in the table: risk factor.

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Reference-table entries

XRCC3Risk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 14:104165753
Cytoband: 14q32.33
HGVS: NM_005432.4(XRCC3):c.722C>T (p.Thr241Met)
Allele change: Silent

Associated conditions / phenotypes

Melanoma, cutaneous malignant, susceptibility to, 6

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.