ClinVar Miner

List of variants in gene CHD8 reported as likely pathogenic 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.3308G>T (p.Gly1103Val)	rs1064795655
NM_001170629.2(CHD8):c.3519-2A>G	rs1594344233

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