List of variants in gene CHD2 reported as not provided for electroclinical syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001271.4(CHD2):c.557T>C (p.Val186Ala)	rs760795656	0.00001
NM_001271.4(CHD2):c.3702A>C (p.Lys1234Asn)
NM_001271.4(CHD2):c.4921C>T (p.Gln1641Ter)	rs864309548
NM_001271.4(CHD2):c.5035C>T (p.Arg1679Ter)	rs797044912
NM_001271.4(CHD2):c.5202A>C (p.Gln1734His)	rs1009699195

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