List of variants in gene FOXP1 studied for Intellectual disability

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001349338.3(FOXP1):c.119A>T (p.Glu40Val)	rs765070623	0.00004
NM_001349338.3(FOXP1):c.1652+4C>T	rs572849158	0.00001
NM_001349338.3(FOXP1):c.1000G>C (p.Asp334His)	rs1576028676
NM_001349338.3(FOXP1):c.1183G>A (p.Ala395Thr)	rs376351360
NM_001349338.3(FOXP1):c.1350A>T (p.Ala450=)	rs2037865324
NM_001349338.3(FOXP1):c.1393A>G (p.Arg465Gly)	rs869025202
NM_001349338.3(FOXP1):c.1426C>T (p.Gln476Ter)	rs2107310122
NM_001349338.3(FOXP1):c.1541G>A (p.Arg514His)	rs797045586
NM_001349338.3(FOXP1):c.1652+5G>C	rs794727216
NM_001349338.3(FOXP1):c.1888G>T (p.Val630Leu)	rs772816590

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