ClinVar Miner

List of variants in gene NF2 reported as likely benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_000268.4(NF2):c.*2841C>T rs142797364 0.00410
NM_000268.4(NF2):c.*1618T>C rs184477204 0.00213
NM_000268.4(NF2):c.*2311G>A rs113956497 0.00203
NM_000268.4(NF2):c.1123-6C>T rs147898623 0.00173
NM_000268.4(NF2):c.*1438A>G rs376061969 0.00167
NM_000268.4(NF2):c.12C>T (p.Ala4=) rs144477078 0.00115
NM_000268.4(NF2):c.1113C>T (p.Asn371=) rs142459414 0.00033
NM_000268.4(NF2):c.*2487A>G rs550207111 0.00029
NM_000268.4(NF2):c.240+15C>T rs200701337 0.00014
NM_000268.4(NF2):c.1439C>T (p.Thr480Met) rs145666157 0.00013
NM_000268.4(NF2):c.1392G>A (p.Ala464=) rs375819833 0.00006
NM_000268.4(NF2):c.*704del rs567370520 0.00004
NM_000268.4(NF2):c.1774T>C (p.Phe592Leu) rs764972504 0.00003
NM_000268.4(NF2):c.*2113C>T rs537244098 0.00002
NM_000268.4(NF2):c.599+3G>A rs768301915 0.00002
NM_000268.4(NF2):c.*1320_*1325del rs148703036
NM_000268.4(NF2):c.*2369T>C rs150581809
NM_000268.4(NF2):c.*3603A>C rs557359614
NM_000268.4(NF2):c.*52C>A rs370016332

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