"Genome Diagnostics Laboratory, The Hospital for Sick Children"[submit - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 284044	NM_001457.4(FLNB):c.2493C>T (p.Pro831=)	FLNB, LOC129936935	Single nucleotide variant (synonymous variant)	FLNB-Related Spectrum Disorders +3 more	GBenign/Likely benign
Select item 346323	NM_001457.4(FLNB):c.2523T>G (p.Pro841=)	FLNB, LOC129936935	Single nucleotide variant (synonymous variant)	FLNB-Related Spectrum Disorders +7 more	GBenign/Likely benign