Variant (rsID / SNP)

rs147537388

rs147537388 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FOXP1. Location: chromosome 3, position 71,015,105. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

FOXP1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:71015105
Cytoband: 3p13
HGVS: NM_001349338.3(FOXP1):c.1825G>A (p.Ala609Thr)
Allele change: Missense_A608T

Associated conditions / phenotypes

History of neurodevelopmental disorder

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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