List of variants in gene NF2 reported by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000268.4(NF2):c.1123-6C>T	rs147898623	0.00173
NM_000268.4(NF2):c.*4G>A	rs141099051	0.00165
NM_000268.4(NF2):c.1386C>T (p.Arg462=)	rs138354622	0.00086
NM_000268.4(NF2):c.1416C>T (p.Leu472=)	rs148776784	0.00081
NM_000268.4(NF2):c.1113C>T (p.Asn371=)	rs142459414	0.00033
NM_000268.4(NF2):c.1340+8G>T	rs370604189	0.00029
NM_000268.4(NF2):c.613A>G (p.Met205Val)	rs141629512	0.00016
NM_000268.4(NF2):c.1311A>G (p.Ala437=)	rs144628209	0.00001
NM_000268.4(NF2):c.115-1G>A	rs2065657938
NM_000268.4(NF2):c.169C>T (p.Arg57Ter)	rs121434259
NM_000268.4(NF2):c.586C>T (p.Arg196Ter)	rs1555993336

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