List of variants in gene PGK1 reported as likely benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000291.4(PGK1):c.1214-178C>T	rs138797609	0.02691
NM_000291.4(PGK1):c.1213+167C>T	rs150219676	0.01251
NC_000023.11:g.78104207G>C	rs182927805	0.00402
NM_000291.4(PGK1):c.641+51A>G	rs144954339	0.00295
NM_000291.4(PGK1):c.116+49C>T	rs373135293	0.00234
NM_000291.4(PGK1):c.273-27A>G	rs138345294	0.00115
NM_000291.4(PGK1):c.1048C>T (p.Arg350Trp)	rs183087139	0.00074
NM_000291.4(PGK1):c.846G>C (p.Leu282Phe)	rs782668224	0.00007
NC_000023.11:g.78104069T>A	rs150921338
NC_000023.11:g.78104244C>G	rs187835265

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