ClinVar Miner

List of variants reported as benign for Neurofibromatosis, type 2 by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 16
Download table as spreadsheet
HGVS dbSNP
NM_000268.4(NF2):c.107A>G (p.Asn36Ser) rs372279458
NM_000268.4(NF2):c.1113C>T (p.Asn371=) rs142459414
NM_000268.4(NF2):c.12C>T (p.Ala4=) rs144477078
NM_000268.4(NF2):c.1340+8G>T rs370604189
NM_000268.4(NF2):c.1341-7C>T rs574718828
NM_000268.4(NF2):c.1386C>T (p.Arg462=) rs138354622
NM_000268.4(NF2):c.1416C>T (p.Leu472=) rs148776784
NM_000268.4(NF2):c.1439C>T (p.Thr480Met) rs145666157
NM_000268.4(NF2):c.1451T>C (p.Met484Thr) rs141538143
NM_000268.4(NF2):c.1749G>A (p.Gln583=) rs201911915
NM_000268.4(NF2):c.1752C>T (p.Ser584=) rs370999558
NM_000268.4(NF2):c.240+15C>T rs200701337
NM_000268.4(NF2):c.246G>A (p.Leu82=) rs371270318
NM_000268.4(NF2):c.465C>T (p.Pro155=) rs374911526
NM_000268.4(NF2):c.613A>G (p.Met205Val) rs141629512
NM_016418.5(NF2):c.1123-6C>T rs147898623

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.