List of variants in gene combination CYGB, PRCD reported as likely pathogenic 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001077620.3(PRCD):c.74+1G>A	rs779066277	0.00001
NM_001077620.3(PRCD):c.102_111dup (p.Ser38Ter)
NM_001077620.3(PRCD):c.2T>C (p.Met1Thr)	rs527236092
NM_001077620.3(PRCD):c.9del (p.Thr4fs)

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