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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 516655	NM_005378.6(MYCN):c.18G>A (p.Thr6=)	MYCN, MYCNOS (V98I)	Single nucleotide variant (synonymous variant +2 more)	not provided +2 more	GLikely benign
Select item 517759	NM_005378.6(MYCN):c.69G>T (p.Ser23=)	MYCN, MYCNOS	Single nucleotide variant (synonymous variant +2 more)	Feingold syndrome type 1 +1 more	GBenign/Likely benign
Select item 703188	NM_005378.6(MYCN):c.279G>A (p.Glu93=)	MYCNOS, MYCN	Single nucleotide variant (non-coding transcript variant +3 more)	not provided +1 more	GLikely benign

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