List of variants in gene PCCB reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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_000532.5(PCCB):c.815G>A (p.Arg272Gln)	rs150555106	0.00158
NM_000532.5(PCCB):c.563G>C (p.Gly188Ala)	rs796052024	0.00001
NM_000532.5(PCCB):c.1220G>A (p.Gly407Asp)	rs2529972037
NM_000532.5(PCCB):c.652A>G (p.Lys218Glu)	rs781576125

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