List of variants in gene CPS1 reported as not provided for inborn disorder of amino acid metabolism

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_001875.5(CPS1):c.637G>A (p.Gly213Ser)	rs138392504	0.00102
NM_001875.5(CPS1):c.2809_2810del (p.Ile937fs)	rs1318756445	0.00001

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