ClinVar Miner

List of variants in gene TNRC6A reported as uncertain significance for Epilepsy, familial adult myoclonic, 6

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Minimum conflict level: Report conflict between different conditions
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: 2

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HGVS	dbSNP	gnomAD frequency
NM_014494.4(TNRC6A):c.136AAG[1] (p.Lys47del)	rs2151408186
NM_014494.4(TNRC6A):c.3838-10G>T	rs760665329

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