List of variants in gene combination ALDOA, LOC112694756 reported as uncertain significance 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001243177.4(ALDOA):c.922G>A (p.Val308Ile)	rs142759891	0.00013
NM_001243177.4(ALDOA):c.764G>A (p.Arg255His)	rs534264493	0.00004
NM_001243177.4(ALDOA):c.929C>T (p.Ala310Val)	rs201658390	0.00004
NM_001243177.4(ALDOA):c.1073G>A (p.Arg358Gln)	rs1332829045

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