List of variants in gene PPP3CA reported as likely pathogenic by GeneDx

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000944.5(PPP3CA):c.1340-2A>G	rs1553920188
NM_000944.5(PPP3CA):c.1394del (p.His465fs)	rs1578382902
NM_000944.5(PPP3CA):c.322C>T (p.Pro108Ser)
NM_000944.5(PPP3CA):c.352G>A (p.Asp118Asn)
NM_000944.5(PPP3CA):c.480C>A (p.Phe160Leu)
NM_000944.5(PPP3CA):c.762G>T (p.Arg254Ser)	rs1334933549

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