Variants in gene NCF2 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 4

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HGVS	dbSNP
NM_000433.3(NCF2):c.1081A>T (p.Thr361Ser)	rs147744729
NM_000433.3(NCF2):c.563G>A (p.Arg188Lys)	rs115365142
NM_000433.4(NCF2):c.298C>G (p.Gln100Glu)	rs119103276
NM_000433.4(NCF2):c.918G>A (p.Gln306=)	rs535561432

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