List of variants in gene CHD8 reported as likely benign for intellectual developmental disorder with autism and macrocephaly

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001170629.2(CHD8):c.4809G>A (p.Ala1603=)	rs61736703	0.00383
NM_001170629.2(CHD8):c.2907+12A>T	rs200189975	0.00186
NM_001170629.2(CHD8):c.6119A>G (p.Asp2040Gly)	rs148494847	0.00048
NM_001170629.2(CHD8):c.161G>T (p.Gly54Val)	rs1057519411
NM_001170629.2(CHD8):c.4762A>T (p.Arg1588Trp)	rs1057519410

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