ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_000268.4(NF2):c.*2876T>C rs5763431 0.31213
NM_000268.4(NF2):c.*2468C>G rs1034880 0.30558
NM_000268.4(NF2):c.*354T>C rs1008515 0.23305
NM_000268.4(NF2):c.*1208C>T rs2530680 0.23028
NM_000268.4(NF2):c.*1904A>G rs73390944 0.15076
NM_000268.4(NF2):c.*3274G>A rs11090576 0.14218
NM_000268.4(NF2):c.*2235G>A rs5997506 0.14204
NM_000268.4(NF2):c.*1792G>A rs17462054 0.09370
NM_000268.4(NF2):c.*2224A>G rs112175950 0.07518
NM_000268.4(NF2):c.*974C>T rs8140096 0.05362
NM_000268.4(NF2):c.*2759G>A rs5763430 0.04278
NM_000268.4(NF2):c.*3575G>A rs41278851 0.01965
NM_000268.4(NF2):c.*1640A>C rs138312881 0.01614
NM_000268.4(NF2):c.*2455T>C rs73159090 0.01308
NM_000268.4(NF2):c.*2922G>A rs112930471 0.01227
NM_000268.4(NF2):c.*2408G>A rs114416141 0.01032
NM_000268.4(NF2):c.*1270T>C rs542927614 0.00992
NM_000268.4(NF2):c.*3208G>A rs117863523 0.00549
NM_000268.4(NF2):c.*1087C>T rs148973148 0.00248
NM_000268.4(NF2):c.*4G>A rs141099051 0.00165
NM_000268.4(NF2):c.*720G>A rs184043147 0.00065
NM_000268.4(NF2):c.886-15C>T rs200837904 0.00030
NM_000268.4(NF2):c.-18G>A rs201591536 0.00026
NM_000268.4(NF2):c.246G>A (p.Leu82=) rs371270318 0.00021
NM_000268.4(NF2):c.*503C>T rs191509325 0.00016
NM_000268.4(NF2):c.1540A>G (p.Met514Val) rs201527155 0.00009
NM_000268.4(NF2):c.*2032dup rs11442202
NM_000268.4(NF2):c.*2077C>T rs144993615

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