Variant (rsID / SNP)

rs139871607

rs139871607 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AXIN2. Location: chromosome 17, position 63,534,353. Clinical significance in the table: Benign/Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

AXIN2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:63534353
Cytoband: 17q24.1
HGVS: NM_004655.4(AXIN2):c.1168A>G (p.Ser390Gly)
Allele change: Missense_S390G

Associated conditions / phenotypes

Oligodontia-cancer predisposition syndrome|Oligodontia|Colorectal cancer|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.