List of variants in gene FLNA reported as uncertain significance by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001110556.2(FLNA):c.4451A>G (p.Gln1484Arg)	rs200130356	0.00081
NM_001110556.2(FLNA):c.3995A>G (p.Asp1332Gly)	rs200615848	0.00018
NM_001110556.2(FLNA):c.4528A>C (p.Asn1510His)	rs1557177310
NM_001110556.2(FLNA):c.6146G>A (p.Arg2049His)	rs1557176118
NM_001110556.2(FLNA):c.6199G>A (p.Glu2067Lys)	rs1557176102
NM_001110556.2(FLNA):c.6532G>C (p.Val2178Leu)	rs1569551461

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