C0220687[trait identifier] AND "Rady Children's Institute for Genomic - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2584454	NM_013275.6(ANKRD11):c.1974_1977dup (p.Glu660fs)	ANKRD11 (E660fs)	Microsatellite (frameshift variant)	KBG syndrome	GLikely pathogenic
Select item 279678	NM_013275.6(ANKRD11):c.1903_1907del (p.Lys635fs)	ANKRD11 (K635fs)	Microsatellite (frameshift variant)	not provided +11 more	GPathogenic/Likely pathogenic
Select item 2584471	NM_013275.6(ANKRD11):c.1616_1617del (p.Thr539fs)	ANKRD11 (T539fs)	Microsatellite (frameshift variant)	KBG syndrome	GPathogenic

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