List of variants in gene combination ALDH5A1, GPLD1, LOC129995978 reported as likely benign by PreventionGenetics, part of Exact Sciences

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_001080.3(ALDH5A1):c.130C>G (p.Leu44Val)	rs185042766	0.00250
NM_001080.3(ALDH5A1):c.175C>T (p.Leu59=)	rs907112605	0.00032
NM_001080.3(ALDH5A1):c.-9G>A	rs2532810543
NM_001080.3(ALDH5A1):c.102C>G (p.Ala34=)	rs779034609

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