RS752704782 FOXP2

Health Risk Chr 7:114631527
Upload your DNA to see your genotype for this variant.
Associated Conditions
Inborn genetic diseases
Childhood apraxia of speech
Inborn genetic diseases
Childhood apraxia of speech
Other Variants in FOXP2
rs121908377 rs121908378 rs786200976 rs199581885 rs201649896 rs201320940 rs759778893 rs147624408 rs117662905 rs1064793842
Ask Dr. Hemsworth about this variant