"PreventionGenetics, part of Exact Sciences"[submitter] AND "ZNHIT3"[g - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 784743	NM_004773.4(ZNHIT3):c.21C>T (p.Ser7=)	ZNHIT3	Single nucleotide variant (synonymous variant +1 more)	ZNHIT3-related disorder +2 more	GBenign/Likely benign
Select item 3036460	NM_001163735.2(MYO19):c.2757+674_2757+676dup	MYO19, ZNHIT3	Duplication (intron variant)	ZNHIT3-related disorder	GLikely benign
Select item 3056481	NM_001163735.2(MYO19):c.2757+541G>A	MYO19, ZNHIT3 (Q136*)	Single nucleotide variant (nonsense +2 more)	ZNHIT3-related disorder	GBenign

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