List of variants in gene combination LOC106029312, NCF1 reported as uncertain significance for immune system disorder

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000265.7(NCF1):c.292T>G (p.Cys98Gly)	rs144018361	0.00124
NM_000265.7(NCF1):c.269G>A (p.Arg90His)	rs201802880	0.00110
NM_000265.7(NCF1):c.108G>A (p.Ser36=)	rs146173318	0.00031
NM_000265.7(NCF1):c.575-6G>A
NM_000265.7(NCF1):c.682+5C>T

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