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Gene entry

FOXP1

forkhead box P1

Chromosome
3
Cytoband
3p13
Variants (rsID)
132

FOXP1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p13). Its official name is “forkhead box P1”. The reference table lists 132 variants (rsID) for this gene.

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Clinically classified variants

12 reference-table entries with clinical significance.

  • rs146606219Benignsingle nucleotide variantHistory of neurodevelopmental disorder
  • rs147537388Benignsingle nucleotide variantHistory of neurodevelopmental disorder
  • rs200643313Conflicting interpretationssingle nucleotide variantHistory of neurodevelopmental disorder
  • rs202173892Conflicting interpretationssingle nucleotide variantHistory of neurodevelopmental disorder
  • rs532329866Conflicting interpretationssingle nucleotide variantHistory of neurodevelopmental disorder|Intellectual disability-severe speech delay-mild dysmorphism syndrome|Cerebellar vermis hypoplasia|Intellectual disability-severe speech delay-mild dysmorphism syndrome|Congenital cerebellar hypoplasia
  • rs794727216Conflicting interpretationssingle nucleotide variantIntellectual disability-severe speech delay-mild dysmorphism syndrome
  • rs76145927Likely benignsingle nucleotide variant
  • rs794727155Pathogenicsingle nucleotide variant
  • rs797045584Pathogenicsingle nucleotide variantIntellectual disability-severe speech delay-mild dysmorphism syndrome
  • rs797045586Pathogenicsingle nucleotide variantIntellectual disability-severe speech delay-mild dysmorphism syndrome|Inborn genetic diseases|Intellectual disability|See cases
  • rs869025202Pathogenicsingle nucleotide variantIntellectual disability-severe speech delay-mild dysmorphism syndrome|Intellectual disability
  • rs869025203Pathogenicsingle nucleotide variantIntellectual disability-severe speech delay-mild dysmorphism syndrome

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.