List of variants in gene SLC25A22 reported as uncertain significance for Early Infantile Epileptic Encephalopathy, Autosomal Recessive

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001191061.2(SLC25A22):c.*560C>T	rs556969774	0.00010
NM_001191061.2(SLC25A22):c.*780C>T	rs886048693	0.00003
NM_001191061.2(SLC25A22):c.861C>T (p.Gly287=)	rs202218399	0.00001
NM_001191061.2(SLC25A22):c.*1418AATA[2]	rs755572915
NM_001191061.2(SLC25A22):c.*209A>G	rs537403010
NM_001191061.2(SLC25A22):c.-138_-137insC	rs886048701
NM_001191061.2(SLC25A22):c.-72TCCACC[4]	rs145401722

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