Variants in gene MEGF10 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: 18

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HGVS	dbSNP	gnomAD frequency
NM_001256545.2(MEGF10):c.609C>T (p.Cys203=)	rs113794264	0.00845
NM_001256545.2(MEGF10):c.1046G>A (p.Arg349His)	rs78847357	0.00577
NM_001256545.2(MEGF10):c.489C>T (p.Ile163=)	rs34649270	0.00577
NM_001256545.2(MEGF10):c.2757C>T (p.Asn919=)	rs36061366	0.00492
NM_001256545.2(MEGF10):c.303C>T (p.Ser101=)	rs77203884	0.00260
NM_001256545.2(MEGF10):c.1002C>T (p.His334=)	rs142947482	0.00254
NM_001256545.2(MEGF10):c.1500G>A (p.Gln500=)	rs146075981	0.00243
NM_001256545.2(MEGF10):c.2463C>T (p.Pro821=)	rs139929890	0.00229
NM_001256545.2(MEGF10):c.2654G>A (p.Gly885Glu)	rs116500162	0.00227
NM_001256545.2(MEGF10):c.3003C>T (p.Ser1001=)	rs35159176	0.00207
NM_001256545.2(MEGF10):c.1564G>A (p.Gly522Arg)	rs140563851	0.00178
NM_001256545.2(MEGF10):c.2857-8T>G	rs201148765	0.00117
NM_001256545.2(MEGF10):c.1602C>T (p.Tyr534=)	rs114704569	0.00116
NM_001256545.2(MEGF10):c.3026-8C>T	rs185480820	0.00098
NM_001256545.2(MEGF10):c.117-5_117-4insC	rs538399152	0.00081
NM_001256545.2(MEGF10):c.2175C>T (p.Ser725=)	rs558369303	0.00006
NM_001256545.2(MEGF10):c.522G>A (p.Arg174=)	rs201076330	0.00005
NM_001256545.2(MEGF10):c.1800C>T (p.Cys600=)	rs528654275	0.00004

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