C0424503[trait identifier] AND "Laboratory of Medical Genetics, Univer - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 1710149	NM_201599.3(ZMYM3):c.1322G>A (p.Arg441Gln)	ZMYM3 (R441Q)	Single nucleotide variant (missense variant)	Abnormal facial shape +3 more	GUncertain significance
Select item 1710148	NM_001303512.2(PDZD4):c.2208G>C (p.Lys736Asn)	PDZD4 (K621N +5 more)	Single nucleotide variant (missense variant)	Hand tremor +4 more	GUncertain significance

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