ClinVar Miner

List of variants reported as uncertain significance 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.7327C>T (p.Arg2443Cys)	rs766886630	0.00002
NM_001271938.2(MEGF8):c.7269+5G>A
NM_001271938.2(MEGF8):c.8338G>A (p.Val2780Met)
NM_004753.7(DHRS3):c.730G>C (p.Glu244Gln)

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