List of variants in gene CHD4 reported as likely pathogenic by University of Washington Center for Mendelian Genomics, University of Washington

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001273.5(CHD4):c.5273A>G (p.Tyr1758Cys)	rs777021265	0.00004
NM_001273.5(CHD4):c.1481C>T (p.Thr494Met)	rs375234607	0.00002
NM_001273.5(CHD4):c.5221A>G (p.Ile1741Val)	rs1229933151	0.00002
NM_001273.5(CHD4):c.5638C>T (p.Pro1880Ser)	rs1947956104	0.00001
NM_001273.5(CHD4):c.1686+1G>T	rs1948532502
NM_001273.5(CHD4):c.22C>T (p.Pro8Ser)	rs1948698590
NM_001273.5(CHD4):c.3533C>T (p.Ala1178Val)	rs1435884753

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