List of variants in gene NF1 reported as likely benign by Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001042492.3(NF1):c.528T>A (p.Asp176Glu)	rs112306990	0.00380
NM_001042492.3(NF1):c.7531G>C (p.Val2511Leu)	rs2230850	0.00189
NM_001042492.3(NF1):c.3468C>T (p.Asn1156=)	rs147955381	0.00083

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