Variant (rsID / SNP)
rs869025202
rs869025202 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FOXP1. Location: chromosome 3, position 71,026,829. Clinical significance in the table: Pathogenic/Likely pathogenic.
Reference-table entries
FOXP1Pathogenic
- Clinical significance (as recorded)
- Pathogenic/Likely pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:71026829
- Cytoband
- 3p13
- HGVS
- NM_001349338.3(FOXP1):c.1393A>G (p.Arg465Gly)
- Allele change
- Missense_R464G
Associated conditions / phenotypes
Intellectual disability-severe speech delay-mild dysmorphism syndrome|Intellectual disability
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.