List of variants in gene SBF2 reported as benign for Charcot-Marie-Tooth disease

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: 10

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HGVS	dbSNP
NM_030962.3(SBF2):c.1173A>G (p.Ala391=)	rs79470805
NM_030962.3(SBF2):c.3646C>G (p.Gln1216Glu)	rs12574508
NM_030962.3(SBF2):c.3794-20C>T	rs116966215
NM_030962.3(SBF2):c.4533A>G (p.Thr1511=)	rs79251068
NM_030962.3(SBF2):c.4571-6C>T	rs2645029
NM_030962.3(SBF2):c.4933-15T>C	rs75447733
NM_030962.3(SBF2):c.513+17G>C	rs73410819
NM_030962.3(SBF2):c.753-16T>A	rs7128234
NM_030962.3(SBF2):c.909C>T (p.Pro303=)	rs16907355
NM_030962.3(SBF2):c.93T>C (p.Phe31=)	rs200263159

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