List of variants in gene CDT1 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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.613G>A (p.Gly205Ser)	rs145552478	0.00292
NM_030928.4(CDT1):c.841G>A (p.Gly281Arg)	rs368718178	0.00001
NM_030928.4(CDT1):c.352-7C>G

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