List of variants in gene NCF2 reported as not provided for hematologic disorder

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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000433.4(NCF2):c.230G>A (p.Arg77Gln)	rs119103275	0.00001
NM_000433.4(NCF2):c.383C>T (p.Ala128Val)	rs119103274	0.00001
NM_000433.4(NCF2):c.551G>C (p.Arg184Pro)	rs137854518	0.00001
NM_000433.4(NCF2):c.605C>T (p.Ala202Val)	rs137854508	0.00001
NM_000433.4(NCF2):c.125A>G (p.Asn42Ser)	rs137854514
NM_000433.4(NCF2):c.130G>C (p.Gly44Arg)	rs137854510
NM_000433.4(NCF2):c.130G>T (p.Gly44Cys)	rs137854510
NM_000433.4(NCF2):c.233G>A (p.Gly78Glu)	rs137854519
NM_000433.4(NCF2):c.279C>G (p.Asp93Glu)	rs137854507
NM_000433.4(NCF2):c.305G>C (p.Arg102Pro)	rs137854515
NM_000433.4(NCF2):c.323A>T (p.Asp108Val)	rs137854509
NM_000433.4(NCF2):c.409T>A (p.Trp137Arg)	rs137854516
NM_000433.4(NCF2):c.419C>A (p.Ala140Asp)	rs137854520
NM_000433.4(NCF2):c.505C>G (p.Gln169Glu)	rs137854517

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