ClinVar Miner

List of variants reported as likely benign for Intellectual disability, autosomal dominant 38; Developmental and epileptic encephalopathy, 33

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001958.5(EEF1A2):c.1266C>A (p.Gly422=)	rs202102758	0.00277
NM_001958.5(EEF1A2):c.183C>T (p.Asp61=)	rs147929770	0.00008
NM_001958.5(EEF1A2):c.1182G>T (p.Leu394=)	rs199643016	0.00006

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