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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 24

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HGVS	dbSNP	gnomAD frequency
NM_001256545.2(MEGF10):c.3216G>C (p.Arg1072Ser)	rs75783175	0.00171
NM_001256545.2(MEGF10):c.1626C>T (p.Cys542=)	rs146902993	0.00129
NM_001256545.2(MEGF10):c.1975+10G>A	rs148814585	0.00080
NM_001256545.2(MEGF10):c.1130+3G>A	rs115184652	0.00076
NM_001256545.2(MEGF10):c.1841-5T>C	rs372378202	0.00032
NM_001256545.2(MEGF10):c.50G>A (p.Cys17Tyr)	rs145733370	0.00023
NM_001256545.2(MEGF10):c.2176G>A (p.Ala726Thr)	rs139884665	0.00016
NM_001256545.2(MEGF10):c.2980+14A>G	rs370563737	0.00014
NM_001256545.2(MEGF10):c.2157T>C (p.His719=)	rs374544972	0.00009
NM_001256545.2(MEGF10):c.2289C>T (p.Asn763=)	rs151316424	0.00009
NM_001256545.2(MEGF10):c.2442T>C (p.Thr814=)	rs370850456	0.00009
NM_001256545.2(MEGF10):c.2943G>A (p.Pro981=)	rs371253627	0.00009
NM_001256545.2(MEGF10):c.417C>T (p.Cys139=)	rs148349018	0.00006
NM_001256545.2(MEGF10):c.1080C>T (p.Tyr360=)	rs751813170	0.00005
NM_001256545.2(MEGF10):c.3180A>G (p.Pro1060=)	rs144450528	0.00005
NM_001256545.2(MEGF10):c.781-15T>C	rs767842462	0.00003
NM_001256545.2(MEGF10):c.2919G>A (p.Val973=)	rs770936974	0.00002
NM_001256545.2(MEGF10):c.1008C>T (p.Ser336=)	rs145815113	0.00001
NM_001256545.2(MEGF10):c.1215C>T (p.Tyr405=)	rs781762135	0.00001
NM_001256545.2(MEGF10):c.789G>A (p.Val263=)	rs1188804374	0.00001
NM_001256545.2(MEGF10):c.951C>T (p.Gly317=)	rs145870973	0.00001
NM_001256545.2(MEGF10):c.1673G>T (p.Arg558Leu)	rs182243856
NM_001256545.2(MEGF10):c.3215_3216delinsAC (p.Arg1072Asn)	rs386692223
NM_001256545.2(MEGF10):c.954T>C (p.Val318=)	rs1580833127

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