"PreventionGenetics, part of Exact Sciences"[submitter] AND "TM4SF19-D - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 779236	NM_152773.5(DYNLT2B):c.57G>A (p.Glu19=)	DYNLT2B, LOC129938285 +1 more	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 3058419	NM_152773.5(DYNLT2B):c.-4dup	DYNLT2B, LOC129938285 +1 more	Duplication (5 prime UTR variant)	DYNLT2B-related condition	GLikely benign