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

Minimum submission review status:		Collection method:
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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_015937.6(PIGT):c.634C>T (p.His212Tyr)	rs574183358	0.00009
NM_015937.6(PIGT):c.949A>G (p.Ile317Val)	rs773624614	0.00003
NM_015937.6(PIGT):c.1072G>A (p.Val358Met)	rs370184382
NM_015937.6(PIGT):c.602T>C (p.Leu201Pro)	rs1555876854

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