Gene entry
FOXP2
forkhead box P2
- Chromosome
- 7
- Cytoband
- 7q31.1
- Variants (rsID)
- 82
FOXP2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7q31.1). Its official name is “forkhead box P2”. The reference table lists 82 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs10244649Benignsingle nucleotide variantChildhood apraxia of speech
- rs201649896Conflicting interpretationssingle nucleotide variantChildhood apraxia of speech
- rs766476648Uncertain significancesingle nucleotide variantChildhood apraxia of speech
Other listed variants
- rs1194328
- rs1456029
- rs1528090
- rs1563408
- rs1830198
- rs1852470
- rs1868757
- rs2049602
- rs2189012
- rs2244419
- rs2396720
- rs2396721
- rs2694932
- rs2694933
- rs2694943
- rs4727799
- rs4730626
- rs6969188
- rs7784315
- rs7785799
- rs10230087
- rs10249531
- rs11981044
- rs12154391
- rs12673879
- rs12705960
- rs13228816
- rs17136908
- rs17372211
- rs17508329
- rs34658162
- rs60336079
- rs62467872
- rs62469198
- rs72603563
- rs72603568
- rs73208664
- rs73208672
- rs74382451
- rs74878988
- rs75124371
- rs75192965
- rs75461445
- rs76100638
- rs76853245
- rs77221237
- rs77823977
- rs78398868
- rs78447914
- rs78607823
- rs78908968
- rs79244337
- rs79793367
- rs79863212
- rs80006872
- rs113269040
- rs116869628
- rs116961407
- rs117327635
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.