List of variants in gene NF2 reported as pathogenic for schwannoma

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
NC_000022.11:g.(29668447_29671826)_(29681601_?)del
NM_000268.4(NF2):c.125_126insG (p.Gly43fs)	rs587776564
NM_000268.4(NF2):c.205_211del (p.Lys69fs)	rs587776565
NM_000268.4(NF2):c.363+1G>A	rs1601583839
NM_000268.4(NF2):c.448-1G>A	rs2146966216

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