Variant (rsID / SNP)

rs876659460

rs876659460 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APC. Location: chromosome 5, position 112,170,806. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

APCLikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 5:112170806
Cytoband: 5q22.2
HGVS: NM_000038.6(APC):c.1902T>G (p.Ser634Arg)
Allele change: Missense_S634R

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome

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.