List of variants in gene PIGT reported as uncertain significance for Multiple congenital anomalies-hypotonia-seizures syndrome 3; Paroxysmal nocturnal hemoglobinuria 2

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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.634C>T (p.His212Tyr)	rs574183358	0.00009
NM_015937.6(PIGT):c.949A>G (p.Ile317Val)	rs773624614	0.00003
NM_015937.6(PIGT):c.1252C>G (p.Pro418Ala)

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