List of variants in gene CCDC146 reported as pathogenic by Genetics of Infertility and Preimplantation Genetic Diagnosis, Centre Hospitalier Universitaire Grenoble Alpes

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_020879.3(CCDC146):c.1084C>T (p.Arg362Ter)	rs371350411	0.00007
NM_020879.3(CCDC146):c.1084C>G (p.Arg362Gly)	rs371350411
NM_020879.3(CCDC146):c.2112del (p.Arg704fs)	rs1327651159

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