ClinVar Miner

List of variants in gene NF2 reported as benign for Neurofibromatosis, type 2

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 26
Download table as spreadsheet
NM_000268.3(NF2):c.*1208C>T rs2530680
NM_000268.3(NF2):c.*1792G>A rs17462054
NM_000268.3(NF2):c.*1904A>G rs73390944
NM_000268.3(NF2):c.*2032dupT rs11442202
NM_000268.3(NF2):c.*2224A>G rs112175950
NM_000268.3(NF2):c.*2235G>A rs5997506
NM_000268.3(NF2):c.*2468C>G rs1034880
NM_000268.3(NF2):c.*2759G>A rs5763430
NM_000268.3(NF2):c.*2876T>C rs5763431
NM_000268.3(NF2):c.*3274G>A rs11090576
NM_000268.3(NF2):c.*354T>C rs1008515
NM_000268.3(NF2):c.*974C>T rs8140096
NM_000268.3(NF2):c.-110G>C rs1800540
NM_000268.3(NF2):c.-204C>A rs1800539
NM_000268.3(NF2):c.-246C>G rs56733822
NM_000268.3(NF2):c.107A>G (p.Asn36Ser) rs372279458
NM_000268.3(NF2):c.1113C>T (p.Asn371=) rs142459414
NM_000268.3(NF2):c.1123-6C>T rs147898623
NM_000268.3(NF2):c.12C>T (p.Ala4=) rs144477078
NM_000268.3(NF2):c.1340+8G>T rs370604189
NM_000268.3(NF2):c.1386C>T (p.Arg462=) rs138354622
NM_000268.3(NF2):c.1416C>T (p.Leu472=) rs148776784
NM_000268.3(NF2):c.1451T>C (p.Met484Thr) rs141538143
NM_000268.3(NF2):c.1752C>T (p.Ser584=) rs370999558
NM_000268.3(NF2):c.246G>A (p.Leu82=) rs371270318
NM_000268.3(NF2):c.613A>G (p.Met205Val) rs141629512

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.