RS201649896 FOXP2

Health Risk Chr 7:114426561
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What This Variant Does
"CLNSIG=255
Associated Conditions
Childhood apraxia of speech
Inborn genetic diseases
FOXP2-related disorder
Childhood apraxia of speech
Inborn genetic diseases
FOXP2-related disorder
Other Variants in FOXP2
rs121908377 rs121908378 rs786200976 rs199581885 rs201320940 rs759778893 rs147624408 rs117662905 rs1064793842 rs1135401820
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