List of variants in gene NF1 reported as uncertain significance by Revvity Omics, Revvity

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001042492.3(NF1):c.107C>G (p.Thr36Ser)	rs199966218	0.00015
NM_001042492.3(NF1):c.7213A>G (p.Ile2405Val)	rs565708398	0.00001
NM_001042492.3(NF1):c.7891A>G (p.Thr2631Ala)	rs199474793	0.00001
NM_001042492.3(NF1):c.3137C>G (p.Thr1046Arg)	rs2151432404
NM_001042492.3(NF1):c.415T>G (p.Ser139Ala)	rs1555606096
NM_001042492.3(NF1):c.494C>G (p.Thr165Ser)	rs876660009
NM_001042492.3(NF1):c.5625TCT[1] (p.Leu1877del)	rs1131691081
NM_001042492.3(NF1):c.6299T>G (p.Leu2100Arg)	rs1555534708
NM_001042492.3(NF1):c.7381CTT[2] (p.Leu2463del)	rs786203184
NM_001042492.3(NF1):c.7807G>C (p.Val2603Leu)	rs766135206

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