ClinVar Miner

List of variants in gene combination EEF2, LOC130063169 reported as uncertain significance for Spinocerebellar ataxia type 26

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_001961.4(EEF2):c.2241G>A (p.Val747=)	rs772173797	0.00001

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