List of variants in gene DEPDC5 reported as uncertain significance for Focal 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001242896.3(DEPDC5):c.1021G>T (p.Gly341Cys)	rs767594913
NM_001242896.3(DEPDC5):c.1838A>G (p.Asn613Ser)	rs2089445867
NM_001242896.3(DEPDC5):c.4493A>G (p.Asn1498Ser)
NM_001242896.3(DEPDC5):c.4748G>A (p.Arg1583His)	rs2093761069

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