ClinVar Miner

List of variants reported as likely benign for biotinidase deficiency by Illumina Laboratory Services, Illumina

Included ClinVar conditions (1):

Biotinidase deficiency

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001370658.1(BTD):c.-94C>T	rs114567021	0.01730
NM_001370658.1(BTD):c.820A>G (p.Ile274Val)	rs35976361	0.01187

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