ClinVar Miner

List of variants in gene MEGF10 reported as benign for not specified

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Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_001256545.2(MEGF10):c.1114C>T (p.Leu372=) rs31483 0.94572
NM_001256545.2(MEGF10):c.3387T>A (p.Gly1129=) rs3812052 0.48209
NM_001256545.2(MEGF10):c.660-3C>T rs6595769 0.19743
NM_001256545.2(MEGF10):c.1785T>C (p.Pro595=) rs11950427 0.19610
NM_001256545.2(MEGF10):c.588G>A (p.Gln196=) rs3812055 0.16961
NM_001256545.2(MEGF10):c.3215G>A (p.Arg1072Lys) rs17164935 0.14236
NM_001256545.2(MEGF10):c.616G>A (p.Val206Ile) rs3812054 0.10861
NM_001256545.2(MEGF10):c.3162G>A (p.Pro1054=) rs17164938 0.03315
NM_001256545.2(MEGF10):c.116+10T>C rs10519949 0.02763
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.1841-20G>A rs79904777 0.01625
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.1002C>T (p.His334=) rs142947482 0.00254
NM_001256545.2(MEGF10):c.2034C>T (p.Asn678=) rs117124929 0.00145
NM_001256545.2(MEGF10):c.174G>A (p.Thr58=) rs12654455

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