List of variants in gene CDT1 reported as benign for CDT1-related disorder

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_030928.4(CDT1):c.1472G>A (p.Ser491Asn)	rs146199695	0.00536
NM_030928.4(CDT1):c.1221G>A (p.Pro407=)	rs74035838	0.00376
NM_030928.4(CDT1):c.1123-4G>A	rs373938189	0.00137

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