ClinVar Miner

List of variants in gene CHD8 reported as uncertain significance for Autism spectrum disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001170629.2(CHD8):c.7258C>T (p.Arg2420Cys)	rs371294659	0.00001
NM_001170629.2(CHD8):c.3454G>A (p.Val1152Ile)	rs1888123647

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