Variant (rsID / SNP)

rs304731

rs304731 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to XRCC1, PINLYP. Location: chromosome 19, position 44,082,945. The table records no clinical significance for this variant.

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Reference-table entries

XRCC1Not classified

Variant type: upstream_gene_variant
Chromosome / position: 19:44082945
HGVS: NM_006297.3,c.-3335A>G
Allele change: Silent

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.