"Fulgent Genetics, Fulgent Genetics"[submitter] AND "LOC129388665"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 199238	NM_031935.3(HMCN1):c.15010A>T (p.Thr5004Ser)	HMCN1, LOC129388665 (T5004S)	Single nucleotide variant (missense variant)	Age related macular degeneration 1 +2 more	GBenign/Likely benign
Select item 199239	NM_031935.3(HMCN1):c.15011C>T (p.Thr5004Ile)	HMCN1, LOC129388665 (T5004I)	Single nucleotide variant (missense variant)	Age related macular degeneration 1 +2 more	GBenign/Likely benign