List of variants reported as uncertain significance for Childhood apraxia of speech by Revvity Omics, Revvity

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_014491.4(FOXP2):c.1276G>T (p.Val426Leu)	rs761262072	0.00003
NM_014491.4(FOXP2):c.1657C>T (p.Arg553Cys)	rs566961630	0.00001
NM_014491.4(FOXP2):c.1794A>G (p.Ile598Met)	rs565909014	0.00001
NM_014491.4(FOXP2):c.361C>T (p.Leu121Phe)	rs1403341767
NM_014491.4(FOXP2):c.693G>T (p.Gln231His)	rs755829229

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