Variants in gene CHD8 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001170629.2(CHD8):c.1690C>T (p.Arg564Ter)	rs1057524677
NM_001170629.2(CHD8):c.1744C>T (p.Arg582Ter)	rs863224857
NM_001170629.2(CHD8):c.2726C>G (p.Ser909Ter)	rs774906516
NM_001170629.2(CHD8):c.3562C>T (p.Arg1188Ter)	rs1555314911
NM_001170629.2(CHD8):c.4204C>T (p.Arg1402Ter)	rs1334692966
NM_001170629.2(CHD8):c.4373G>A (p.Trp1458Ter)	rs2501888861
NM_001170629.2(CHD8):c.4744C>T (p.Arg1582Ter)	rs1555314211
NM_001170629.2(CHD8):c.4875G>A (p.Trp1625Ter)	rs1555314116
NM_001170629.2(CHD8):c.5326C>T (p.Arg1776Ter)	rs1085307794
NM_001170629.2(CHD8):c.727C>T (p.Arg243Ter)	rs1555318552

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