"Fulgent Genetics, Fulgent Genetics"[submitter] AND "MIR4733HG"[gene] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 322562	NM_001042492.3(NF1):c.-148C>A	LOC111811965, MIR4733HG +1 more	Single nucleotide variant (5 prime UTR variant)	Juvenile myelomonocytic leukemia +4 more	GUncertain significance
Select item 578123	NM_001042492.3(NF1):c.15G>T (p.Arg5Ser)	LOC111811965, MIR4733HG +1 more (R5S)	Single nucleotide variant (missense variant)	Neurofibromatosis, type 1 +4 more	GUncertain significance
Select item 219691	NM_001042492.3(NF1):c.17C>T (p.Pro6Leu)	LOC111811965, MIR4733HG +1 more (P6L)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +6 more	GUncertain significance
Select item 1593023	NM_001042492.3(NF1):c.60+11C>T	LOC111811965, MIR4733HG +1 more	Single nucleotide variant (intron variant)	Neurofibromatosis, familial spinal +4 more	GLikely benign

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