"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "PIGM"[gene - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1170560	NM_145167.3(PIGM):c.999C>T (p.Ser333=)	PIGM	Single nucleotide variant (synonymous variant)	Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency +1 more	GBenign/Likely benign
Select item 2639491	NM_145167.3(PIGM):c.756A>G (p.Glu252=)	PIGM	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 592292	NM_145167.3(PIGM):c.6C>T (p.Gly2=)	PIGM	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign

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ClinVar