List of variants in gene NF1 reported as uncertain significance by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001042492.3(NF1):c.3867C>T (p.Phe1289=)	rs138186428	0.00089
NM_001042492.3(NF1):c.4373A>G (p.Glu1458Gly)	rs878853894	0.00001
NM_001042492.3(NF1):c.7211C>T (p.Ala2404Val)	rs771706364	0.00001
NM_001042492.3(NF1):c.1062+3A>G	rs1057521098
NM_001042492.3(NF1):c.4631C>A (p.Ala1544Glu)	rs1555619015
NM_001042492.3(NF1):c.6623C>G (p.Ala2208Gly)	rs1555534886

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