List of variants in gene NF2 reported as benign by Invitae

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_000268.4(NF2):c.448-17C>T	rs190596693	0.00215
NM_000268.4(NF2):c.1123-6C>T	rs147898623	0.00173
NM_000268.4(NF2):c.12C>T (p.Ala4=)	rs144477078	0.00115
NM_000268.4(NF2):c.1386C>T (p.Arg462=)	rs138354622	0.00086
NM_000268.4(NF2):c.1451T>C (p.Met484Thr)	rs141538143	0.00082
NM_000268.4(NF2):c.1416C>T (p.Leu472=)	rs148776784	0.00081
NM_000268.4(NF2):c.811-17C>G	rs180790168	0.00072
NM_000268.4(NF2):c.1113C>T (p.Asn371=)	rs142459414	0.00033
NM_000268.4(NF2):c.886-15C>T	rs200837904	0.00030
NM_000268.4(NF2):c.1340+8G>T	rs370604189	0.00029
NM_000268.4(NF2):c.246G>A (p.Leu82=)	rs371270318	0.00021
NM_000268.4(NF2):c.114+20G>T	rs746868503	0.00016
NM_000268.4(NF2):c.1749G>A (p.Gln583=)	rs201911915	0.00016
NM_000268.4(NF2):c.613A>G (p.Met205Val)	rs141629512	0.00016
NM_000268.4(NF2):c.107A>G (p.Asn36Ser)	rs372279458	0.00014
NM_000268.4(NF2):c.240+15C>T	rs200701337	0.00014
NM_000268.4(NF2):c.1439C>T (p.Thr480Met)	rs145666157	0.00013
NM_000268.4(NF2):c.465C>T (p.Pro155=)	rs374911526	0.00011
NM_000268.4(NF2):c.999+15G>A	rs367716680	0.00011
NM_000268.4(NF2):c.1447-11C>T	rs571246532	0.00002
NM_000268.4(NF2):c.1752C>T (p.Ser584=)	rs370999558	0.00001
NM_000268.4(NF2):c.114+19del
NM_000268.4(NF2):c.1341-7C>T	rs574718828
NM_000268.4(NF2):c.1446+13del	rs1195395510
NM_000268.4(NF2):c.363+24dup
NM_000268.4(NF2):c.447+6C>T	rs777369699

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