ClinVar Miner

List of variants in gene NF2 reported as benign

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Gene type:
ClinVar version:
Total variants: 40
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HGVS dbSNP
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.*4G>A rs141099051
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.-752G>C
NM_000268.3(NF2):c.1000-212_1000-210delTAG
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.1123-51C>T
NM_000268.3(NF2):c.1123-6C>T rs147898623
NM_000268.3(NF2):c.115-256A>C
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.1737+1623T>C
NM_000268.3(NF2):c.1752C>T (p.Ser584=) rs370999558
NM_000268.3(NF2):c.241-85G>T
NM_000268.3(NF2):c.246G>A (p.Leu82=) rs371270318
NM_000268.3(NF2):c.364-291C>G
NM_000268.3(NF2):c.364-39A>C rs2530664
NM_000268.3(NF2):c.600-154G>A
NM_000268.3(NF2):c.613A>G (p.Met205Val) rs141629512
NM_000268.3(NF2):c.676-249G>A
NM_000268.3(NF2):c.810+246A>G
NM_000268.3(NF2):c.886-205C>T
NM_000268.3(NF2):c.999+296A>G

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