List of variants reported as uncertain significance for Familial meningioma; Neurofibromatosis, type 2; Schwannomatosis 1 by Fulgent Genetics, Fulgent Genetics

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000268.4(NF2):c.*359G>A	rs572307337	0.00217
NM_000268.4(NF2):c.1619A>G (p.Asn540Ser)	rs774824164	0.00004
NM_000268.4(NF2):c.515G>A (p.Arg172Lys)	rs752963731	0.00002
NM_000268.4(NF2):c.1232G>A (p.Arg411His)	rs201214090	0.00001
NM_000268.4(NF2):c.1701C>G (p.Asp567Glu)	rs1049732514	0.00001
NM_000268.4(NF2):c.674G>A (p.Arg225Gln)	rs543087642	0.00001
NM_000268.4(NF2):c.1243A>G (p.Thr415Ala)	rs776970251
NM_000268.4(NF2):c.215T>C (p.Val72Ala)	rs1260510937

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