List of variants in gene PHEX 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000444.6(PHEX):c.1133T>G (p.Leu378Arg)	rs1930965902
NM_000444.6(PHEX):c.176G>T (p.Cys59Phe)
NM_000444.6(PHEX):c.436+5G>A	rs1602273945

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