ClinVar Miner

List of variants in gene combination KCTD7, LOC129998533 reported as benign for Progressive myoclonic epilepsy type 3

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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: 2

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HGVS	dbSNP	gnomAD frequency
NM_153033.5(KCTD7):c.-44C>T	rs35526611	0.51674
NM_153033.5(KCTD7):c.-116C>T	rs551906037

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