List of variants in gene PIGA reported as uncertain significance by Ambry Genetics

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_002641.4(PIGA):c.61A>G (p.Ser21Gly)	rs375401655	0.00007
NM_002641.4(PIGA):c.877A>G (p.Lys293Glu)	rs202161781	0.00004
NM_002641.4(PIGA):c.1382G>A (p.Arg461Gln)	rs769061128	0.00002
NM_002641.4(PIGA):c.43G>A (p.Ala15Thr)	rs369608621	0.00002
NM_002641.4(PIGA):c.517G>A (p.Val173Met)	rs752395232	0.00002
NM_002641.4(PIGA):c.616A>G (p.Ile206Val)	rs201119959	0.00002
NM_002641.4(PIGA):c.91C>T (p.Arg31Cys)	rs780532806	0.00001
NM_002641.4(PIGA):c.1223C>T (p.Pro408Leu)
NM_002641.4(PIGA):c.1240G>A (p.Asp414Asn)
NM_002641.4(PIGA):c.1424G>T (p.Gly475Val)
NM_002641.4(PIGA):c.407A>G (p.His136Arg)	rs1602212104
NM_002641.4(PIGA):c.823C>T (p.Arg275Trp)	rs1057524256
NM_002641.4(PIGA):c.866C>T (p.Ala289Val)	rs2147717729
NM_002641.4(PIGA):c.955G>A (p.Val319Met)	rs765961204

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