List of variants in gene FOXP1 reported as uncertain significance for not specified

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001349338.3(FOXP1):c.1217C>G (p.Thr406Ser)	rs200355554	0.00016
NM_001349338.3(FOXP1):c.44C>T (p.Ala15Val)	rs532329866	0.00015
NM_001349338.3(FOXP1):c.13T>C (p.Ser5Pro)	rs762898505	0.00012
NM_001349338.3(FOXP1):c.*6G>C	rs373960974	0.00006
NM_001349338.3(FOXP1):c.107G>A (p.Arg36Gln)	rs200643313	0.00005
NM_001349338.3(FOXP1):c.179A>G (p.Gln60Arg)	rs374060287	0.00005
NM_001349338.3(FOXP1):c.181-17952C>T	rs776051503	0.00001
NM_001349338.3(FOXP1):c.1236C>A (p.Ala412=)	rs376833445
NM_001349338.3(FOXP1):c.1277C>T (p.Thr426Ile)
NM_001349338.3(FOXP1):c.1405A>G (p.Thr469Ala)	rs1553668167
NM_001349338.3(FOXP1):c.1652+5G>A	rs794727216
NM_001349338.3(FOXP1):c.181-4C>T	rs558832183
NM_001349338.3(FOXP1):c.274G>C (p.Ala92Pro)	rs1388674903
NM_001349338.3(FOXP1):c.527C>A (p.Thr176Asn)
NM_001349338.3(FOXP1):c.602G>A (p.Arg201His)	rs1450448594

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