Variants in gene MEGF10 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001256545.2(MEGF10):c.3162G>A (p.Pro1054=)	rs17164938	0.03315
NM_001256545.2(MEGF10):c.2199C>T (p.Cys733=)	rs35591368	0.02614
NM_001256545.2(MEGF10):c.2076C>T (p.Pro692=)	rs115309591	0.01810
NM_001256545.2(MEGF10):c.984C>T (p.Asn328=)	rs35550094	0.01638
NM_001256545.2(MEGF10):c.3189G>A (p.Glu1063=)	rs56157640	0.01628
NM_001256545.2(MEGF10):c.218+17C>G	rs72786483	0.00257
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.2034C>T (p.Asn678=)	rs117124929	0.00145
NM_001256545.2(MEGF10):c.3026-8C>T	rs185480820	0.00098
NM_001256545.2(MEGF10):c.1975+10G>A	rs148814585	0.00080

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