List of variants in gene CHD6 reported as likely 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_032221.5(CHD6):c.5577G>A (p.Leu1859=)	rs151251513	0.00067
NM_032221.5(CHD6):c.2997C>T (p.Ser999=)	rs150157135	0.00062
NM_032221.5(CHD6):c.3858C>T (p.Leu1286=)	rs757133401	0.00001
NM_032221.5(CHD6):c.1314+3A>G
NM_032221.5(CHD6):c.3675C>G (p.His1225Gln)
NM_032221.5(CHD6):c.6741A>T (p.Ser2247=)	rs2515869790
NM_032221.5(CHD6):c.948G>A (p.Glu316=)	rs2516565451

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