List of variants in gene CHD3 reported as likely pathogenic by CeGaT Center for Human Genetics Tuebingen

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001005273.3(CHD3):c.3028C>T (p.Arg1010Ter)
NM_001005273.3(CHD3):c.3559C>G (p.Arg1187Gly)
NM_001005273.3(CHD3):c.3608T>C (p.Met1203Thr)	rs1970542838
NM_001005273.3(CHD3):c.4073-2A>C	rs1567864750
NM_001005273.3(CHD3):c.5641C>T (p.Arg1881Cys)

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