ClinVar Miner

List of variants in gene CHD8 reported as not provided for CHD8-Related Disorders

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_001170629.2(CHD8):c.3308G>T (p.Gly1103Val) rs1064795655

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