ClinVar Miner

List of variants in gene NF1 reported as uncertain significance by Blueprint Genetics

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001042492.3(NF1):c.5407A>G (p.Ile1803Val)	rs559910904	0.00001
NM_001042492.3(NF1):c.3061G>C (p.Val1021Leu)	rs1597716939

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