ClinVar Miner

List of variants in gene NF2 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_000268.4(NF2):c.600-194A>G rs2071621 0.00510
NC_000022.11:g.29603369G>C rs112049943 0.00466
NM_000268.4(NF2):c.517-249G>C rs141330612 0.00450
NM_000268.4(NF2):c.885+248C>T rs185240022 0.00376
NM_000268.4(NF2):c.599+289G>A rs187607171 0.00374
NM_000268.4(NF2):c.448-17C>T rs190596693 0.00215
NM_000268.4(NF2):c.1737+2183G>A rs192755300 0.00185
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.517-61G>C rs568134420 0.00136
NM_000268.4(NF2):c.12C>T (p.Ala4=) rs144477078 0.00115
NM_000268.4(NF2):c.675+49T>C rs148076331 0.00098
NM_000268.4(NF2):c.1340+8G>T rs370604189 0.00029
NM_000268.4(NF2):c.-18G>A rs201591536 0.00026
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.363+19C>A rs202225081 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.1385G>A (p.Arg462His) rs373650983 0.00011
NM_000268.4(NF2):c.465C>T (p.Pro155=) rs374911526 0.00011
NM_000268.4(NF2):c.1698C>T (p.Ser566=) rs751987156 0.00005
NM_000268.4(NF2):c.1000-7C>G rs776237839 0.00004
NM_000268.4(NF2):c.325C>T (p.Leu109=) rs201603384 0.00004
NM_000268.4(NF2):c.705A>C (p.Gly235=) rs749331641 0.00003
NM_000268.4(NF2):c.783C>T (p.Ile261=) rs765223726 0.00003
NM_000268.4(NF2):c.1311A>G (p.Ala437=) rs144628209 0.00001
NM_000268.4(NF2):c.1737+300G>T rs139341275
NM_000268.4(NF2):c.364-140dup rs143701873
NM_000268.4(NF2):c.599+280dup rs59436932
NM_000268.4(NF2):c.599+56del rs36029478
NM_000268.4(NF2):c.599+56dup rs36029478
NM_000268.4(NF2):c.600-139G>C rs117536234
NM_000268.4(NF2):c.676-334C>T rs114228106
NM_000268.4(NF2):c.759G>A (p.Lys253=) rs760272926
NM_000268.4(NF2):c.795G>T (p.Ser265=) rs376609988
NM_000268.4(NF2):c.810+23_810+25del rs765519341

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