List of variants in gene combination LOC111811965, MIR4733HG, NF1 reported as uncertain significance for hematologic disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001042492.3(NF1):c.-148C>A	rs886052792	0.00001
NM_001042492.3(NF1):c.15G>T (p.Arg5Ser)	rs1567786804
NM_001042492.3(NF1):c.17C>T (p.Pro6Leu)	rs864622210
NM_001042492.3(NF1):c.46C>G (p.Arg16Gly)
NM_001042492.3(NF1):c.4_5delinsTT (p.Ala2Phe)	rs1555594471

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