Variant (rsID / SNP)
rs114746583
rs114746583 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HOXD10. Location: chromosome 2, position 176,984,006. Clinical significance in the table: Benign.
Reference-table entries
HOXD10Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:176984006
- Cytoband
- 2q31.1
- HGVS
- NM_002148.4(HOXD10):c.*47G>T
- Allele change
- Silent
Associated conditions / phenotypes
Congenital vertical talus
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.