ClinVar Miner

List of variants in gene combination D2HGDH, LOC129936033 reported as benign for 2-hydroxyglutaric aciduria

Included ClinVar conditions (6):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_152783.5(D2HGDH):c.292+28T>G	rs62191977	0.74780
NM_152783.5(D2HGDH):c.292+9G>A	rs148813816	0.02496

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