ClinVar Miner

List of variants in gene BCKDHB reported as likely benign by Counsyl

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_183050.4(BCKDHB):c.951+27209A>G	rs207467187
NM_183050.4(BCKDHB):c.952-16_952-15del	rs890103324

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