ClinVar Miner

List of variants in gene CDT1 reported as uncertain significance by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_030928.4(CDT1):c.610G>A (p.Val204Met)	rs773495319	0.00001
NM_030928.4(CDT1):c.1381C>A (p.Leu461Met)	rs2508214380

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