"GeneDx"[submitter] AND "LOC126860116"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2575561	NM_005221.6(DLX5):c.570del (p.Lys191fs)	DLX5, LOC126860116 (K191fs)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 1186365	NM_005221.6(DLX5):c.540+227C>T	DLX5, LOC126860116	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1241509	NM_005221.6(DLX5):c.540+91T>C	DLX5, LOC126860116	Single nucleotide variant (intron variant)	not provided	GBenign

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