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

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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: 12

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HGVS	dbSNP	gnomAD frequency
NM_014491.4(FOXP2):c.50A>T (p.Gln17Leu)	rs201649896	0.00034
NM_014491.4(FOXP2):c.1937A>G (p.Asn646Ser)	rs145154396	0.00026
NM_014491.4(FOXP2):c.*2302G>A	rs192272516	0.00021
NM_014491.4(FOXP2):c.*2017del	rs377464931	0.00009
NM_014491.4(FOXP2):c.*832A>C	rs769641895	0.00009
NM_014491.4(FOXP2):c.1494T>C (p.Tyr498=)	rs191237950	0.00007
NM_014491.4(FOXP2):c.1569G>A (p.Arg523=)	rs376776032	0.00005
NM_014491.4(FOXP2):c.2103C>T (p.Asp701=)	rs559347815	0.00005
NM_014491.4(FOXP2):c.*188CTT[5]	rs770516756
NM_014491.4(FOXP2):c.3279_3280dup	rs777898958
NM_014491.4(FOXP2):c.483ACAACAGCAGCA[3] (p.Gln188_Gln191dup)	rs761316361
NM_014491.4(FOXP2):c.510ACA[4] (p.Gln191del)	rs398124272

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