List of variants in gene PIGT studied for anemia

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_015937.6(PIGT):c.1620T>C (p.Tyr540=)	rs707577	0.76713
NM_015937.6(PIGT):c.1400+48T>C	rs2741566	0.73775
NM_015937.6(PIGT):c.1371G>A (p.Thr457=)	rs13217	0.38173
NM_015937.6(PIGT):c.969C>T (p.Thr323=)	rs116312756	0.00428
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.1252C>G (p.Pro418Ala)
NM_015937.6(PIGT):c.1401-2A>G	rs587777028
NM_015937.6(PIGT):c.197del (p.Tyr66fs)	rs1555876283
NM_015937.6(PIGT):c.594+36dup	rs3092108
NM_015937.6(PIGT):c.602T>C (p.Leu201Pro)	rs1555876854
NM_015937.6(PIGT):c.767_770del (p.Lys256fs)	rs776974834

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