List of variants in gene CHD3 reported as benign 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.3825C>T (p.Asp1275=)	rs61744840	0.00743
NM_001005273.3(CHD3):c.1815C>T (p.Asp605=)	rs140662047	0.00244
NM_001005273.3(CHD3):c.3318C>T (p.Ile1106=)
NM_001005273.3(CHD3):c.5027-3C>T
NM_001005273.3(CHD3):c.721G>A (p.Ala241Thr)

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