List of variants in gene combination LOC130005303, SBF2 reported as uncertain significance for Charcot-Marie-Tooth disease type 4B2

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_030962.4(SBF2):c.-101A>C	rs886047577	0.00017
NM_030962.4(SBF2):c.48G>A (p.Glu16=)	rs889453292	0.00003
NM_030962.4(SBF2):c.-37G>T	rs756232914	0.00002
NM_030962.4(SBF2):c.-106C>T	rs886047578	0.00001
NM_030962.4(SBF2):c.-27C>T	rs1032915786	0.00001
NM_030962.4(SBF2):c.-49G>A	rs1476971148	0.00001
NM_030962.4(SBF2):c.-64C>T	rs1010047569	0.00001
NM_030962.4(SBF2):c.23T>G (p.Phe8Cys)	rs886047576

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