C0342573[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1635025	NM_000515.5(GH1):c.456+19G>T	GH-LCR, GH1	Single nucleotide variant (intron variant)	not provided +4 more	GBenign/Likely benign
Select item 15970	NM_000515.5(GH1):c.291+1G>A	GH-LCR, GH1	Single nucleotide variant (intron variant +1 more)	Short stature due to growth hormone qualitative anomaly +4 more	GPathogenic
Select item 284727	NM_000515.5(GH1):c.116C>T (p.Ala39Val)	GH-LCR, GH1 (A39V)	Single nucleotide variant (missense variant)	GH1-related disorder +7 more	GBenign/Likely benign

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