Variant (rsID / SNP)

rs766476648

rs766476648 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FOXP2. Location: chromosome 7, position 114,303,524. Clinical significance in the table: Uncertain significance.

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Reference-table entries

FOXP2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 7:114303524
Cytoband: 7q31.1
HGVS: NM_014491.4(FOXP2):c.1789A>C (p.Asn597His)
Allele change: Silent

Associated conditions / phenotypes

Childhood apraxia of speech

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.