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

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001042492.3(NF1):c.6172A>G (p.Ile2058Val)	rs201712827	0.00017
NM_001042492.3(NF1):c.3722G>A (p.Arg1241Gln)	rs543387071	0.00001
NM_001042492.3(NF1):c.1260+6T>A
NM_001042492.3(NF1):c.1527+1187C>G
NM_001042492.3(NF1):c.4672C>T (p.His1558Tyr)	rs1468638747

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