ClinVar Miner

List of variants in gene CHD8, LOC126861888 studied for autism, susceptiblity to

Included ClinVar conditions (22):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001170629.2(CHD8):c.6795C>T (p.Phe2265=)	rs747289672
NM_001170629.2(CHD8):c.6853AAG[2] (p.Lys2287del)	rs755776815
NM_001170629.2(CHD8):c.7054C>T (p.Arg2352Ter)

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