Variants in gene combination CDKL5, RS1 with conflicting interpretations reported as "uncertain significance and "likely pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000330.4(RS1):c.251C>G (p.Ser84Cys)	rs1338396929
NM_000330.4(RS1):c.404G>C (p.Gly135Ala)	rs61752152
NM_000330.4(RS1):c.673T>C (p.Ter225Arg)	rs1057517433

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