ClinVar Miner

List of variants in gene NCF4 reported as likely pathogenic by Fulgent Genetics, Fulgent Genetics

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000631.5(NCF4):c.529-2A>T	rs199890705	0.00002
NM_000631.5(NCF4):c.32+2T>C
NM_000631.5(NCF4):c.3G>A (p.Met1Ile)

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