ClinVar Miner

List of variants reported as likely benign for phagocytic cell dysfunction by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Included ClinVar conditions (21):

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_000397.4(CYBB):c.654C>A (p.Gly218=)	rs35080474	0.00285
NM_000397.4(CYBB):c.66C>T (p.Asn22=)	rs193922450	0.00006

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