Variant (rsID / SNP)

rs1799782

rs1799782 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to XRCC1. Location: chromosome 19, position 44,057,574. Clinical significance in the table: Benign.

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Reference-table entries

XRCC1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:44057574
Cytoband: 19q13.31
HGVS: NM_006297.3(XRCC1):c.580C>T (p.Arg194Trp)
Allele change: Missense_R194W

Associated conditions / phenotypes

Non-small cell lung carcinoma

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.