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Variant (rsID / SNP)

rs202173892

FOXP1

rs202173892 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FOXP1. Location: chromosome 3, position 71,015,168. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

FOXP1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
3:71015168
Cytoband
3p13
HGVS
NM_001349338.3(FOXP1):c.1762G>A (p.Ala588Thr)
Allele change
Missense_A587T

Associated conditions / phenotypes

History of neurodevelopmental disorder

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.