ClinVar Miner

List of variants in gene combination ATP10A, GABRA5, GABRB3 reported as pathogenic for Epilepsy, childhood absence, susceptibility to, 1; Epilepsy, childhood absence, susceptibility to, 5

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NC_000015.10:g.(?_25862297)_(26937328_?)del

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