ClinVar Miner

List of variants in gene CDKL5 reported as likely pathogenic by Undiagnosed Diseases Network, NIH

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001323289.2(CDKL5):c.2762_2763del (p.Thr921fs)	rs1927146242
NM_001323289.2(CDKL5):c.2828_2829del (p.Arg943fs)	rs1555955290

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