List of variants reported as likely pathogenic by Wilkie Group, Clinical Genetics Lab, WIMM, University of Oxford

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001271938.2(MEGF8):c.4697G>A (p.Arg1566His)	rs397515427	0.00001
NM_001271938.2(MEGF8):c.7948GTCTTCTTCTCC[1] (p.2650VFFS[1])	rs2514360670
NM_001271938.2(MEGF8):c.7961TCT[2] (p.Phe2656del)	rs2514360725
NM_001271938.2(MEGF8):c.878T>C (p.Leu293Pro)

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