Variants in gene CHD2 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001271.4(CHD2):c.1934C>T (p.Thr645Met)	rs2053619460
NM_001271.4(CHD2):c.2095C>T (p.Arg699Trp)
NM_001271.4(CHD2):c.2699G>A (p.Arg900Gln)	rs1567149946
NM_001271.4(CHD2):c.2705A>G (p.His902Arg)	rs2053935622
NM_001271.4(CHD2):c.3454C>T (p.Arg1152Trp)	rs1596443241
NM_001271.4(CHD2):c.3782G>T (p.Trp1261Leu)	rs1555444603
NM_001271.4(CHD2):c.4492C>T (p.Gln1498Ter)
NM_001271.4(CHD2):c.4971G>A (p.Trp1657Ter)	rs398122998

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