ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
Download table as spreadsheet
NM_000268.3(NF2):c.114+20G>T rs746868503
NM_000268.3(NF2):c.363+19C>A rs202225081
NM_000268.3(NF2):c.448-17C>T rs190596693
NM_000268.4(NF2):c.-18G>A rs201591536
NM_000268.4(NF2):c.12C>T (p.Ala4=) rs144477078
NM_000268.4(NF2):c.1311A>G (p.Ala437=) rs144628209
NM_000268.4(NF2):c.1340+8G>T rs370604189
NM_000268.4(NF2):c.1470G>A (p.Pro490=) rs373442542
NM_000268.4(NF2):c.1749G>A (p.Gln583=) rs201911915
NM_000268.4(NF2):c.325C>T (p.Leu109=) rs201603384
NM_000268.4(NF2):c.465C>T (p.Pro155=) rs374911526
NM_000268.4(NF2):c.705A>C (p.Gly235=) rs749331641
NM_000268.4(NF2):c.759G>A (p.Lys253=) rs760272926
NM_000268.4(NF2):c.795G>T (p.Ser265=) rs376609988
NM_016418.5(NF2):c.1000-7C>G rs776237839

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.