ClinVar Miner

List of variants in gene NF1 reported as uncertain significance by Institute of Human Genetics, Cologne University

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.2410-13A>G	rs1567848711
NM_001042492.3(NF1):c.4903_4917dup (p.Tyr1639_Glu1640insTyrAlaLysProTyr)	rs2069327013

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