"Illumina Laboratory Services, Illumina"[submitter] AND "MIR484"[gene] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 884574	NM_001143979.1(NDE1):c.-794C>T	MIR484, NDE1	Single nucleotide variant (non-coding transcript variant)	Lissencephaly 4	GUncertain significance
Select item 318016	NM_001143979.1(NDE1):c.-773G>A	MIR484, NDE1	Single nucleotide variant (non-coding transcript variant)	Lissencephaly 4	GLikely benign
Select item 884575	NM_001143979.1(NDE1):c.-765C>T	MIR484, NDE1	Single nucleotide variant (non-coding transcript variant)	Lissencephaly 4	GUncertain significance
Select item 318017	NM_001143979.1(NDE1):c.-741dup	MIR484, NDE1	Duplication (non-coding transcript variant)	Lissencephaly, Recessive	GUncertain significance

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