List of variants in gene CHD2 reported as uncertain significance by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001271.4(CHD2):c.4534C>T (p.Arg1512Trp)	rs755898320	0.00006
NM_001271.4(CHD2):c.5245C>T (p.Pro1749Ser)	rs772907727	0.00002
NM_001271.4(CHD2):c.1052+14C>G	rs146319346	0.00001

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