"Fulgent Genetics, Fulgent Genetics"[submitter] AND "FBLN5"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 5481	NM_006329.4(FBLN5):c.1051C>T (p.Arg351Trp)	FBLN5 (R351W +3 more)	Single nucleotide variant (missense variant)	Macular degeneration, age-related, 3 +7 more	GUncertain significance
Select item 1172837	NM_006329.4(FBLN5):c.245A>C (p.Asn82Thr)	FBLN5 (N123T +3 more)	Single nucleotide variant (missense variant)	Macular degeneration, age-related, 3 +3 more	GUncertain significance