ClinVar Miner

List of variants reported as benign for Epileptic encephalopathy, childhood-onset

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Total variants: 5
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HGVS dbSNP
NM_001271.4(CHD2):c.1995G>A (p.Pro665=) rs747900073
NM_001271.4(CHD2):c.4219T>A (p.Ser1407Thr) rs61756301
NM_001271.4(CHD2):c.4527C>T (p.Ile1509=) rs34315566
NM_001271.4(CHD2):c.4721G>C (p.Gly1574Ala) rs56227200
NM_001271.4(CHD2):c.4874A>G (p.Asn1625Ser) rs143431217

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