List of variants in gene PIGT reported as risk factor for 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_015937.6(PIGT):c.1401-2A>G	rs587777028
NM_015937.6(PIGT):c.197del (p.Tyr66fs)	rs1555876283
NM_015937.6(PIGT):c.767_770del (p.Lys256fs)	rs776974834

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