List of variants in gene NF2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 31

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HGVS	dbSNP	gnomAD frequency
NM_000268.4(NF2):c.*359G>A	rs572307337	0.00217
NM_000268.4(NF2):c.*1618T>C	rs184477204	0.00213
NM_000268.4(NF2):c.*2311G>A	rs113956497	0.00203
NM_000268.4(NF2):c.1123-6C>T	rs147898623	0.00173
NM_000268.4(NF2):c.1737+2098A>G	rs75296199	0.00053
NM_000268.4(NF2):c.1113C>T (p.Asn371=)	rs142459414	0.00033
NM_000268.4(NF2):c.*3133A>G	rs527795536	0.00032
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.1749G>A (p.Gln583=)	rs201911915	0.00016
NM_000268.4(NF2):c.240+15C>T	rs200701337	0.00014
NM_000268.4(NF2):c.465C>T (p.Pro155=)	rs374911526	0.00011
NM_000268.4(NF2):c.771G>A (p.Pro257=)	rs759032771	0.00010
NM_000268.4(NF2):c.1206C>T (p.Ala402=)	rs137953976	0.00009
NM_000268.4(NF2):c.1392G>A (p.Ala464=)	rs375819833	0.00006
NM_000268.4(NF2):c.1000-7C>G	rs776237839	0.00004
NM_000268.4(NF2):c.255T>C (p.Asp85=)	rs375802248	0.00004
NM_000268.4(NF2):c.576C>T (p.Tyr192=)	rs149803133	0.00004
NM_000268.4(NF2):c.783C>T (p.Ile261=)	rs765223726	0.00003
NM_000268.4(NF2):c.912T>C (p.His304=)	rs200272173	0.00003
NM_000268.4(NF2):c.651C>T (p.Tyr217=)	rs367802186	0.00002
NM_000268.4(NF2):c.861C>T (p.Ser287=)	rs143160499	0.00002
NM_000268.4(NF2):c.1128G>C (p.Arg376=)	rs757322524	0.00001
NM_000268.4(NF2):c.*2369T>C	rs150581809
NM_000268.4(NF2):c.*3303G>A
NM_000268.4(NF2):c.1281G>A (p.Glu427=)
NM_000268.4(NF2):c.1291C>T (p.Leu431=)	rs1297186898
NM_000268.4(NF2):c.1293G>A (p.Leu431=)	rs1340711783
NM_000268.4(NF2):c.1714A>C (p.Ser572Arg)	rs1379683835
NM_000268.4(NF2):c.450T>C (p.Tyr150=)	rs2146966255
NM_000268.4(NF2):c.735C>T (p.Asp245=)

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