Variants in gene CFH 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_000186.4(CFH):c.1204C>T (p.His402Tyr)	rs1061170	0.63625
NM_000186.4(CFH):c.2850G>T (p.Gln950His)	rs149474608	0.00425
NM_000186.4(CFH):c.245-15T>C	rs200079172	0.00052
NM_000186.4(CFH):c.285T>C (p.Thr95=)	rs148182625	0.00049
NM_000186.4(CFH):c.172T>G (p.Ser58Ala)	rs141336681	0.00047
NM_000186.4(CFH):c.2957-7A>G	rs190778135	0.00031
NM_000186.4(CFH):c.1418C>T (p.Ala473Val)	rs371053403	0.00006
NM_000186.4(CFH):c.2196G>A (p.Thr732=)	rs144325643	0.00006
NM_000186.4(CFH):c.1736T>C (p.Val579Ala)	rs201411537	0.00004
NM_000186.4(CFH):c.770G>A (p.Arg257His)	rs140107330	0.00003
NM_000186.4(CFH):c.16A>G (p.Lys6Glu)	rs749875053	0.00002
NM_000186.4(CFH):c.2424A>G (p.Ile808Met)	rs752302466	0.00002
NM_000186.4(CFH):c.2944C>T (p.Pro982Ser)	rs149938052	0.00001
NM_000186.4(CFH):c.879G>A (p.Gln293=)	rs769615121	0.00001
NM_000186.4(CFH):c.2783-3del	rs748791414
NM_000186.4(CFH):c.2956+13G>A	rs572034879
NM_000186.4(CFH):c.3134-5T>C	rs513699

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