List of variants in gene combination LOC111811965, MIR4733HG, NF1 reported as uncertain significance by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001042492.3(NF1):c.17C>G (p.Pro6Arg)	rs864622210	0.00001
NM_001042492.3(NF1):c.30C>G (p.Val10=)	rs1033348008	0.00001
NM_001042492.3(NF1):c.13A>G (p.Arg5Gly)	rs1598173775
NM_001042492.3(NF1):c.29T>G (p.Val10Gly)	rs2143145014
NM_001042492.3(NF1):c.38T>C (p.Val13Ala)	rs1911556061
NM_001042492.3(NF1):c.41T>A (p.Val14Asp)	rs2143145332
NM_001042492.3(NF1):c.46C>T (p.Arg16Cys)	rs1057520334
NM_001042492.3(NF1):c.4_5delinsTT (p.Ala2Phe)	rs1555594471
NM_001042492.3(NF1):c.5C>A (p.Ala2Asp)	rs1555594473

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