ClinVar Miner

List of variants in gene NF2 reported as likely benign for not specified

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Total variants: 15
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HGVS dbSNP
NM_000268.3(NF2):c.1000-7C>G rs776237839
NM_000268.3(NF2):c.114+20G>T rs746868503
NM_000268.3(NF2):c.12C>T (p.Ala4=) rs144477078
NM_000268.3(NF2):c.1311A>G (p.Ala437=) rs144628209
NM_000268.3(NF2):c.1340+8G>T rs370604189
NM_000268.3(NF2):c.1749G>A (p.Gln583=) rs201911915
NM_000268.3(NF2):c.325C>T (p.Leu109=) rs201603384
NM_000268.3(NF2):c.363+19C>A rs202225081
NM_000268.3(NF2):c.705A>C (p.Gly235=) rs749331641
NM_000268.3(NF2):c.759G>A (p.Lys253=) rs760272926
NM_000268.3(NF2):c.795G>T (p.Ser265=) rs376609988
NM_181832.2(NF2):c.-18G>A rs201591536
NM_181832.2(NF2):c.1470G>A (p.Pro490=) rs373442542
NM_181832.2(NF2):c.448-17C>T rs190596693
NM_181832.2(NF2):c.465C>T (p.Pro155=) rs374911526

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