"Fulgent Genetics, Fulgent Genetics"[submitter] AND "LOC122861289"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 758619	NM_212482.4(FN1):c.1638C>T (p.Phe546=)	FN1, LOC122861289	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 752916	NM_212482.4(FN1):c.1626C>T (p.Asn542=)	FN1, LOC122861289	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 717899	NM_212482.4(FN1):c.1547-6A>G	FN1, LOC122861289	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign

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