List of variants in gene NCF4 reported as benign by PreventionGenetics, part of Exact Sciences

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000631.5(NCF4):c.758+57T>C	rs2075939	0.86715
NM_000631.5(NCF4):c.528+16A>G	rs2072708	0.64364
NM_000631.5(NCF4):c.897G>A (p.Ser299=)	rs11552115	0.12037
NM_000631.5(NCF4):c.735C>T (p.Tyr245=)	rs2072712	0.11870
NM_000631.5(NCF4):c.69G>A (p.Ser23=)	rs10854695	0.04124
NM_000631.5(NCF4):c.628-14C>A	rs56071149	0.01126
NM_000631.5(NCF4):c.343-4A>G	rs79312013	0.00334
NM_000631.5(NCF4):c.528+18G>C	rs6000455

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