RS201320940 FOXP2

Health Risk Chr 7:114658261
Upload your DNA to see your genotype for this variant.
Associated Conditions
Childhood apraxia of speech
Inborn genetic diseases
Childhood apraxia of speech
Inborn genetic diseases
Other Variants in FOXP2
rs121908377 rs121908378 rs786200976 rs199581885 rs201649896 rs759778893 rs147624408 rs117662905 rs1064793842 rs1135401820
Ask Dr. Hemsworth about this variant