ClinVar Miner

List of variants reported as pathogenic for childhood apraxia of speech by OMIM

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_014491.4(FOXP2):c.1658G>A (p.Arg553His) rs121908377
NM_014491.4(FOXP2):c.982C>T (p.Arg328Ter) rs121908378

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