ClinVar Miner

List of variants in gene combination CBL, FRA11B, LOC130006894 reported as uncertain significance for Juvenile myelomonocytic leukemia; CBL-related disorder

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_005188.3(CBL):c.-122C>T	rs886047765	0.00029
NM_005188.4(CBL):c.-125_-116delinsT	rs886047763

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