ClinVar Miner

List of variants reported as likely benign for MEGF10-related myopathy by Illumina Laboratory Services, Illumina

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
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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