ClinVar Miner

List of variants in gene CHD7 reported by National Institute on Deafness and Communication Disorders, National Institutes of Health

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_017780.4(CHD7):c.2613+5G>A	rs202143667	0.00008
NM_017780.4(CHD7):c.8276A>G (p.Gln2759Arg)	rs1469714222

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