List of variants in gene combination ALDOA, LOC112694756 reported as 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001365304.2(LOC112694756):c.*489-63G>C	rs9783783	0.52268
NM_001365304.2(LOC112694756):c.150+85_150+86del	rs34855001	0.32000
NM_001365304.2(LOC112694756):c.*1508+17G>T	rs2071390	0.13976
NM_001365304.2(LOC112694756):c.*834-243T>C	rs75721735	0.10199
NM_001365304.2(LOC112694756):c.*1134-40C>T	rs11860935	0.08845
NM_001365304.2(LOC112694756):c.*834-115A>T	rs114445168	0.01746
NM_001243177.4(ALDOA):c.1200C>T (p.Ser400=)	rs77290575	0.01088
NM_001365304.2(LOC112694756):c.150+19G>A	rs41280858	0.00941
NM_001365304.2(LOC112694756):c.*889-16C>A	rs78124282	0.00797
NM_001365304.2(LOC112694756):c.*888+42G>A	rs34429195	0.00445
NM_001365304.2(LOC112694756):c.834-143_834-138del	rs56857043

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