Variants in gene CDKL5 with conflicting interpretations "likely pathogenic" and "uncertain significance"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

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HGVS	dbSNP	gnomAD frequency
NM_001323289.2(CDKL5):c.2684C>T (p.Pro895Leu)	rs587783157	0.00001
NM_001323289.2(CDKL5):c.212A>G (p.Asn71Ser)	rs1925264314
NM_001323289.2(CDKL5):c.2500C>T (p.Gln834Ter)	rs122460158
NM_001323289.2(CDKL5):c.454T>C (p.Cys152Arg)	rs1602272932
NM_001323289.2(CDKL5):c.470C>T (p.Ala157Val)	rs863225066
NM_001323289.2(CDKL5):c.616G>T (p.Asp206Tyr)	rs1555950468
NM_001323289.2(CDKL5):c.65G>A (p.Gly22Glu)	rs1602232972
NM_001323289.2(CDKL5):c.89G>A (p.Cys30Tyr)	rs1555940536

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