List of variants in gene FOXP2 reported as likely pathogenic for specific language disorder

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_014491.4(FOXP2):c.1050G>A (p.Trp350Ter)	rs1349250538	0.00001
NM_014491.4(FOXP2):c.1234C>T (p.Arg412Ter)
NM_014491.4(FOXP2):c.1418G>A (p.Gly473Glu)
NM_014491.4(FOXP2):c.1426C>T (p.Arg476Ter)	rs1178491246
NM_014491.4(FOXP2):c.1658G>A (p.Arg553His)	rs121908377
NM_014491.4(FOXP2):c.1719G>A (p.Trp573Ter)
NM_014491.4(FOXP2):c.1747C>T (p.Arg583Ter)
NM_014491.4(FOXP2):c.1769+2T>C	rs1135401820
NM_014491.4(FOXP2):c.360_373del (p.Leu121fs)

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