Variant (rsID / SNP)

rs17104965

rs17104965 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PAX9. Location: chromosome 14, position 37,145,916. Clinical significance in the table: Benign.

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Reference-table entries

PAX9Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 14:37145916
Cytoband: 14q13.3
HGVS: NM_001372076.1(PAX9):c.*259C>T
Allele change: Silent

Associated conditions / phenotypes

Tooth agenesis, selective, 3

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.