ClinVar Miner

List of variants reported as likely benign for Neurofibromatosis, type 2 by Illumina Clinical Services Laboratory,Illumina

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Minimum conflict level:
ClinVar version:
Total variants: 19
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HGVS dbSNP
NM_000268.4(NF2):c.*1320_*1325del rs148703036
NM_000268.4(NF2):c.*1438A>G rs376061969
NM_000268.4(NF2):c.*1618T>C rs184477204
NM_000268.4(NF2):c.*2113C>T rs537244098
NM_000268.4(NF2):c.*2311G>A rs113956497
NM_000268.4(NF2):c.*2369T>C rs150581809
NM_000268.4(NF2):c.*2487A>G rs550207111
NM_000268.4(NF2):c.*2841C>T rs142797364
NM_000268.4(NF2):c.*3603A>C rs557359614
NM_000268.4(NF2):c.*52C>A rs370016332
NM_000268.4(NF2):c.*704del rs567370520
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.1392G>A (p.Ala464=) rs375819833
NM_000268.4(NF2):c.1439C>T (p.Thr480Met) rs145666157
NM_000268.4(NF2):c.1774T>C (p.Phe592Leu) rs764972504
NM_000268.4(NF2):c.240+15C>T rs200701337
NM_016418.5(NF2):c.1123-6C>T rs147898623
NM_016418.5(NF2):c.599+3G>A rs768301915

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