RS121908378 FOXP2

Health Risk Chr 7:114642616
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What This Variant Does
"rs121908378, also known as Arg328Ter or R328X, is a C-to-T transition in exon 7 of the FOXP2 gene. A...
Associated Conditions
Childhood apraxia of speech
Inborn genetic diseases
See cases
Childhood apraxia of speech
Inborn genetic diseases
See cases
Other Variants in FOXP2
rs121908377 rs786200976 rs199581885 rs201649896 rs201320940 rs759778893 rs147624408 rs117662905 rs1064793842 rs1135401820
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