List of variants in gene combination DBNL, LOC129998341, PGAM2 reported as likely benign for disorder of glycolysis

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000290.4(PGAM2):c.480T>C (p.Ile160=)	rs780650903	0.00011
NM_000290.4(PGAM2):c.489C>T (p.Ala163=)	rs1201379677
NM_000290.4(PGAM2):c.504C>T (p.Asn168=)
NM_000290.4(PGAM2):c.511A>G (p.Ile171Val)	rs372452057

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