List of variants in gene PIGA reported as uncertain significance for anemia

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_002641.4(PIGA):c.849-19C>T	rs780237513	0.00002
NM_002641.4(PIGA):c.1048C>T (p.Pro350Ser)	rs372966902
NM_002641.4(PIGA):c.142G>A (p.Gly48Ser)
NM_002641.4(PIGA):c.167T>C (p.Leu56Pro)
NM_002641.4(PIGA):c.248T>C (p.Leu83Pro)	rs1569180063

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