List of variants in gene combination DBNL, LOC129998342, PGAM2 reported as 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000290.4(PGAM2):c.341T>G (p.Ile114Ser)	rs61756062	0.02444
NM_000290.4(PGAM2):c.366G>A (p.Pro122=)	rs143830182	0.00529
NM_000290.4(PGAM2):c.375G>A (p.Pro125=)	rs145985559	0.00382

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