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Variant (rsID / SNP)

rs149764887

AXIN2

rs149764887 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AXIN2. Location: chromosome 17, position 63,533,469. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

AXIN2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
17:63533469
Cytoband
17q24.1
HGVS
NM_004655.4(AXIN2):c.1685C>T (p.Pro562Leu)
Allele change
Missense_P562L

Associated conditions / phenotypes

Oligodontia-cancer predisposition syndrome|Hereditary cancer-predisposing syndrome|Colorectal cancer

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.