ClinVar Miner

List of variants in gene combination LOC105369149, SBF2 reported as benign 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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_030962.4(SBF2):c.4571-6C>T	rs2645029	0.87373
NM_030962.4(SBF2):c.4933-15T>C	rs75447733	0.03363

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