ClinVar Miner

List of variants in gene KCTD7 reported as uncertain significance for Unverricht-Lundborg syndrome

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_153033.5(KCTD7):c.*2223_*2226dup rs886062422
NM_153033.5(KCTD7):c.*860CCT[1] rs886062416

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