List of variants in gene FOXP2 reported as likely benign by Eurofins NTD LLC (GA)

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

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_014491.4(FOXP2):c.1843G>A (p.Ala615Thr)	rs182138317	0.00058
NM_014491.4(FOXP2):c.1283G>T (p.Ser428Ile)	rs727503937
NM_014491.4(FOXP2):c.1770-4del	rs398005923
NM_014491.4(FOXP2):c.453GCA[4] (p.Gln191del)	rs776565646
NM_014491.4(FOXP2):c.471GCA[5] (p.Gln191dup)	rs762779073

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