ClinVar Miner

List of variants reported as likely benign for autosomal recessive severe congenital neutropenia by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (7):

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_000760.4(CSF3R):c.2422G>A (p.Glu808Lys)	rs146617729	0.00588
NM_138387.4(G6PC3):c.815A>G (p.Gln272Arg)	rs34491309	0.00334

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