List of variants in gene MEGF10 reported as likely benign by Illumina Laboratory Services, Illumina

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001256545.2(MEGF10):c.*2114T>C	rs77171194	0.05204
NM_001256545.2(MEGF10):c.*1810C>T	rs17685202	0.04703
NM_001256545.2(MEGF10):c.*1410G>T	rs11745840	0.04651
NM_001256545.2(MEGF10):c.3162G>A (p.Pro1054=)	rs17164938	0.03315
NM_001256545.2(MEGF10):c.*1150T>C	rs75528418	0.03313
NM_001256545.2(MEGF10):c.*1522C>A	rs74560067	0.03005
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.*2240G>A	rs77136524	0.01650
NM_001256545.2(MEGF10):c.984C>T (p.Asn328=)	rs35550094	0.01638
NM_001256545.2(MEGF10):c.*534A>G	rs75370992	0.01632
NM_001256545.2(MEGF10):c.3189G>A (p.Glu1063=)	rs56157640	0.01628
NM_001256545.2(MEGF10):c.2034C>T (p.Asn678=)	rs117124929	0.00145
NM_001256545.2(MEGF10):c.*1685G>T	rs17763722	0.00126
NM_001256545.2(MEGF10):c.*3522CA[1]	rs397809018

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