Variant (rsID / SNP)

rs587780608

rs587780608 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APC. Location: chromosome 5, position 112,179,707. Clinical significance in the table: Uncertain significance.

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Reference-table entries

APCUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 5:112179707
Cytoband: 5q22.2
HGVS: NM_000038.6(APC):c.8416C>G (p.Pro2806Ala)
Allele change: Missense_P2806A

Associated conditions / phenotypes

Familial adenomatous polyposis 1|Hereditary cancer-predisposing syndrome|Familial adenomatous polyposis 1

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.