List of variants in gene combination LOC111811965, MIR4733HG, NF1 reported as uncertain significance for neurofibromatosis, familial spinal

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 20

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HGVS	dbSNP	gnomAD frequency
NM_001042492.3(NF1):c.-249_-247dup	rs886052786	0.00018
NM_001042492.3(NF1):c.-229C>G	rs886052789	0.00017
NM_001042492.3(NF1):c.-237C>T	rs878967255	0.00013
NM_001042492.3(NF1):c.-209C>A	rs886052790	0.00002
NM_001042492.3(NF1):c.-251C>T	rs1463146814	0.00002
NM_001042492.3(NF1):c.-51C>T	rs964223360	0.00002
NM_001042492.3(NF1):c.-148C>A	rs886052792	0.00001
NM_001042492.3(NF1):c.-73G>T	rs886052795	0.00001
NM_001042492.3(NF1):c.-84C>T	rs886052794	0.00001
NM_000267.3(NF1):c.-363T>C	rs1911498673
NM_001042492.3(NF1):c.-115T>C	rs886052793
NM_001042492.3(NF1):c.-166T>C	rs1911526241
NM_001042492.3(NF1):c.-173C>G	rs886052791
NM_001042492.3(NF1):c.-237dup	rs886052788
NM_001042492.3(NF1):c.-242dup	rs886052787
NM_001042492.3(NF1):c.-248_-247dup	rs886052786
NM_001042492.3(NF1):c.-265G>C	rs1911511473
NM_001042492.3(NF1):c.-322G>A	rs886052785
NM_001042492.3(NF1):c.15G>T (p.Arg5Ser)	rs1567786804
NM_001042492.3(NF1):c.17C>T (p.Pro6Leu)	rs864622210

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