Variant (rsID / SNP)
rs10244649
rs10244649 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FOXP2. Location: chromosome 7, position 114,333,803. Clinical significance in the table: Benign.
Reference-table entries
FOXP2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:114333803
- Cytoband
- 7q31.1
- HGVS
- NM_014491.4(FOXP2):c.*3822C>T
- Allele change
- Silent
Associated conditions / phenotypes
Childhood apraxia of speech
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.