List of variants studied for phagocytic cell dysfunction by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000265.7(NCF1):c.579G>A (p.Trp193Ter)	rs145360423	0.00054
NM_000631.5(NCF4):c.758+50C>T	rs201021542	0.00011
NM_000101.4(CYBA):c.70G>A (p.Gly24Arg)	rs28941476	0.00001
NM_001098426.2(SMARCD2):c.391C>T (p.Gln131Ter)	rs2040280183	0.00001
NM_000101.4(CYBA):c.288-1G>T	rs111571762
NM_000265.7(NCF1):c.604C>T (p.Arg202Ter)
NM_000265.7(NCF1):c.682+5C>T	rs782219576
NM_000397.4(CYBB):c.626A>G (p.His209Arg)	rs151344482
NM_000631.5(NCF4):c.614_615del (p.Lys205fs)	rs757106743

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