List of variants reported as uncertain significance for Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2 by Illumina Laboratory Services, Illumina

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Total variants: 25

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HGVS	dbSNP	gnomAD frequency
NM_000433.4(NCF2):c.113G>A (p.Arg38Gln)	rs147415774	0.00145
NM_000433.4(NCF2):c.1184G>A (p.Arg395Gln)	rs145229115	0.00131
NM_000433.4(NCF2):c.298C>G (p.Gln100Glu)	rs119103276	0.00019
NM_000433.4(NCF2):c.*97A>C	rs367946786	0.00015
NM_000433.4(NCF2):c.197G>A (p.Arg66Gln)	rs142803799	0.00014
NM_000433.3(NCF2):c.-264C>T	rs150182900	0.00009
NM_000433.4(NCF2):c.636C>T (p.Asp212=)	rs774027102	0.00004
NM_000433.4(NCF2):c.*262C>T	rs201050705	0.00003
NM_000433.4(NCF2):c.837G>A (p.Thr279=)	rs942486247	0.00003
NM_000433.4(NCF2):c.196C>A (p.Arg66=)	rs750782115	0.00002
NM_000433.4(NCF2):c.-98T>C	rs755614780	0.00001
NM_000433.4(NCF2):c.1055A>G (p.Tyr352Cys)	rs748489095	0.00001
NM_000433.4(NCF2):c.1336G>T (p.Asp446Tyr)	rs886045653	0.00001
NM_000433.4(NCF2):c.443C>T (p.Thr148Met)	rs764142541	0.00001
NM_000433.4(NCF2):c.996A>G (p.Ser332=)	rs1192520130	0.00001
NM_000433.4(NCF2):c.1071C>T (p.His357=)	rs1672170931
NM_000433.4(NCF2):c.1084G>A (p.Val362Ile)	rs886045656
NM_000433.4(NCF2):c.1247A>G (p.Gln416Arg)	rs886045655
NM_000433.4(NCF2):c.1291-15C>G	rs886045654
NM_000433.4(NCF2):c.1375G>C (p.Gly459Arg)	rs1671979597
NM_000433.4(NCF2):c.1385T>G (p.Val462Gly)	rs886045652
NM_000433.4(NCF2):c.1498A>G (p.Lys500Glu)	rs886045651
NM_000433.4(NCF2):c.707T>C (p.Ile236Thr)	rs764405660
NM_000433.4(NCF2):c.855+1G>A	rs1352805193
NM_000433.4(NCF2):c.918G>A (p.Gln306=)	rs535561432

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