List of variants in gene GPI reported as pathogenic by OMIM

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000175.5(GPI):c.671C>T (p.Thr224Met)	rs61754634	0.00005
NM_000175.5(GPI):c.475G>A (p.Gly159Ser)	rs137853582	0.00003
NM_000175.5(GPI):c.1028A>G (p.Gln343Arg)	rs267606851	0.00002
NM_000175.5(GPI):c.14C>T (p.Thr5Ile)	rs267606852	0.00001
NM_000175.5(GPI):c.1574T>C (p.Ile525Thr)	rs137853584	0.00001
NM_000175.5(GPI):c.59A>C (p.His20Pro)	rs137853586	0.00001
NM_000175.5(GPI):c.1016T>C (p.Leu339Pro)	rs137853587
NM_000175.5(GPI):c.1040G>A (p.Arg347His)	rs137853583
NM_000175.5(GPI):c.1124C>G (p.Thr375Arg)	rs267606853
NM_000175.5(GPI):c.1615G>A (p.Asp539Asn)	rs137853585

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