ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 32
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HGVS dbSNP
NM_000268.4(NF2):c.*1087C>T rs148973148
NM_000268.4(NF2):c.*1208C>T rs2530680
NM_000268.4(NF2):c.*1270T>C rs542927614
NM_000268.4(NF2):c.*1640A>C rs138312881
NM_000268.4(NF2):c.*1792G>A rs17462054
NM_000268.4(NF2):c.*1904A>G rs73390944
NM_000268.4(NF2):c.*2032dup rs11442202
NM_000268.4(NF2):c.*2077C>T
NM_000268.4(NF2):c.*2224A>G rs112175950
NM_000268.4(NF2):c.*2235G>A rs5997506
NM_000268.4(NF2):c.*2408G>A rs114416141
NM_000268.4(NF2):c.*2455T>C rs73159090
NM_000268.4(NF2):c.*2468C>G rs1034880
NM_000268.4(NF2):c.*2759G>A rs5763430
NM_000268.4(NF2):c.*2876T>C rs5763431
NM_000268.4(NF2):c.*2922G>A rs112930471
NM_000268.4(NF2):c.*3208G>A rs117863523
NM_000268.4(NF2):c.*3274G>A rs11090576
NM_000268.4(NF2):c.*354T>C rs1008515
NM_000268.4(NF2):c.*3575G>A rs41278851
NM_000268.4(NF2):c.*4G>A rs141099051
NM_000268.4(NF2):c.*503C>T rs191509325
NM_000268.4(NF2):c.*720G>A rs184043147
NM_000268.4(NF2):c.*974C>T rs8140096
NM_000268.4(NF2):c.-110G>C rs1800540
NM_000268.4(NF2):c.-18G>A rs201591536
NM_000268.4(NF2):c.-204C>A rs1800539
NM_000268.4(NF2):c.-245C>G rs536438675
NM_000268.4(NF2):c.-246C>G rs56733822
NM_000268.4(NF2):c.1540A>G (p.Met514Val) rs201527155
NM_000268.4(NF2):c.246G>A (p.Leu82=) rs371270318
NM_016418.5(NF2):c.886-15C>T rs200837904

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