List of variants in gene combination PCDHB4, PCDHB@ reported as not provided for epilepsy

Minimum submission review status:		Collection method:
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)
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_018938.4(PCDHB4):c.915del (p.Lys305fs)	rs372292910

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