Variant (rsID / SNP)

rs12452477

rs12452477 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DLX3. Location: chromosome 17, position 48,067,953. Clinical significance in the table: Benign.

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Reference-table entries

DLX3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:48067953
Cytoband: 17q21.33
HGVS: NM_005220.3(DLX3):c.*928A>G
Allele change: Silent

Associated conditions / phenotypes

Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism

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.