List of variants in gene GPI reported as likely pathogenic for hemolytic anemia

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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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.1336C>T (p.Arg446Ter)	rs774419705	0.00004
NM_000175.5(GPI):c.1009G>A (p.Ala337Thr)	rs1238884216	0.00001
NM_000175.5(GPI):c.1574T>C (p.Ile525Thr)	rs137853584	0.00001
NM_000175.5(GPI):c.1648A>G (p.Lys550Glu)	rs933668811	0.00001
NM_000175.5(GPI):c.572A>G (p.His191Arg)	rs758281551	0.00001
NM_000175.5(GPI):c.1040G>A (p.Arg347His)	rs137853583
NM_000175.5(GPI):c.1269+1G>A
NM_000175.5(GPI):c.1498_1501del (p.Val500fs)
NM_000175.5(GPI):c.283-2A>G
NM_000175.5(GPI):c.804+1_804+2del
NM_000175.5(GPI):c.812del (p.Gly271fs)	rs2145419704
NM_000175.5(GPI):c.937_952dup (p.Val318fs)

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