List of variants in gene FOXP1 reported as likely benign for not specified

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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001349338.3(FOXP1):c.1709A>G (p.Asn570Ser)	rs140161845	0.00140
NM_001349338.3(FOXP1):c.1890-5T>C	rs187666567	0.00059
NM_001349338.3(FOXP1):c.1762G>A (p.Ala588Thr)	rs202173892	0.00034
NM_001349338.3(FOXP1):c.855T>G (p.Thr285=)	rs141007926	0.00029
NM_001349338.3(FOXP1):c.936C>T (p.Gly312=)	rs61753356	0.00016
NM_001349338.3(FOXP1):c.44C>T (p.Ala15Val)	rs532329866	0.00015
NM_001349338.3(FOXP1):c.1737G>C (p.Glu579Asp)	rs756328632	0.00005
NM_001349338.3(FOXP1):c.63C>T (p.Gly21=)	rs376702675	0.00005
NM_001349338.3(FOXP1):c.450A>G (p.Gln150=)	rs1433777499	0.00004
NM_001349338.3(FOXP1):c.169C>G (p.Gln57Glu)	rs752141860	0.00003
NM_001349338.3(FOXP1):c.306G>A (p.Met102Ile)	rs749611196	0.00003
NM_001349338.3(FOXP1):c.1328A>G (p.Tyr443Cys)	rs727503936	0.00001
NM_001349338.3(FOXP1):c.126G>A (p.Pro42=)	rs762082081
NM_001349338.3(FOXP1):c.98G>C (p.Arg33Pro)	rs587780339

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