List of variants in gene NF2 reported as benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 36

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HGVS	dbSNP	gnomAD frequency
NM_000268.4(NF2):c.1575-67G>A	rs140086	0.99995
NM_000268.4(NF2):c.240+171T>A	rs2530662	0.67485
NM_000268.4(NF2):c.886-205C>T	rs2252472	0.37694
NM_000268.4(NF2):c.999+296A>G	rs2252587	0.37691
NM_000268.4(NF2):c.600-154G>A	rs2071622	0.37687
NM_000268.4(NF2):c.676-249G>A	rs2857640	0.37672
NM_000268.4(NF2):c.810+246A>G	rs2857641	0.37633
NM_000268.4(NF2):c.241-85G>T	rs5763378	0.32451
NM_000268.4(NF2):c.1737+1623T>C	rs7291645	0.31605
NM_000268.3(NF2):c.-752G>C	rs1800538	0.24203
NM_000268.4(NF2):c.517-150C>T	rs6006220	0.22506
NM_000268.4(NF2):c.364-39A>C	rs2530664	0.14175
NM_000268.4(NF2):c.115-256A>C	rs2531848	0.14159
NM_000268.4(NF2):c.364-291C>G	rs2531849	0.14151
NM_000268.4(NF2):c.1123-51C>T	rs13055076	0.10682
NM_000268.4(NF2):c.1737+135T>C	rs5752952	0.10517
NM_000268.4(NF2):c.1122+129A>T	rs2527336	0.09456
NM_000268.4(NF2):c.1574+173G>A	rs56188151	0.07518
NM_000268.4(NF2):c.241-58G>A	rs79901896	0.06933
NM_000268.4(NF2):c.600-239C>A	rs9614025	0.04215
NM_000268.4(NF2):c.600-215A>G	rs5752949	0.03004
NM_000268.4(NF2):c.1000-212_1000-210del	rs4034748	0.02906
NM_000268.4(NF2):c.1340+248A>G	rs73881591	0.02166
NM_000268.4(NF2):c.114+335dup	rs147717202	0.01672
NM_000268.4(NF2):c.1738-283C>T	rs56761979	0.01470
NM_000268.4(NF2):c.*4G>A	rs141099051	0.00165
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.999+15G>A	rs367716680	0.00011
NC_000022.11:g.29603361del	rs1799754
NC_000022.11:g.29603361dup	rs1799754
NM_000268.4(NF2):c.*3319del	rs372162228
NM_000268.4(NF2):c.1447-222_1447-216dup	rs3074521
NM_000268.4(NF2):c.516+259A>C	rs11913715
NM_000268.4(NF2):c.885+183del	rs35328234
NM_000268.4(NF2):c.886-248GT[3]	rs3842712

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