"Ambry Genetics"[submitter] AND "LOC130003467"[gene] - ClinVar - NCBI

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Items: 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2523070	NR_160800.1(MIR1915HG):n.708C>T	LOC130003467, MIR1915HG	Single nucleotide variant (non-coding transcript variant)	Inborn genetic diseases	GLikely benign
Select item 2493165	NR_160800.1(MIR1915HG):n.642C>G	LOC130003467, MIR1915HG	Single nucleotide variant (non-coding transcript variant)	Inborn genetic diseases	GUncertain significance
Select item 2490924	NR_160800.1(MIR1915HG):n.535G>C	LOC130003467, MIR1915HG	Single nucleotide variant (non-coding transcript variant)	Inborn genetic diseases	GUncertain significance

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