List of variants in gene BCKDHB reported as likely benign by Illumina Laboratory Services, Illumina

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_183050.4(BCKDHB):c.*1798C>T	rs535334878	0.00251
NM_183050.4(BCKDHB):c.*83C>T	rs564127416	0.00052
NM_183050.4(BCKDHB):c.*2072C>T	rs183153737	0.00020
NM_183050.4(BCKDHB):c.63G>T (p.Gly21=)	rs368345065	0.00019
NM_183050.4(BCKDHB):c.987C>T (p.His329=)	rs138670449	0.00019
NM_183050.4(BCKDHB):c.*263C>A	rs533006469

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