ClinVar Miner

List of variants in gene D2HGDH reported as benign by Mendelics

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_152783.5(D2HGDH):c.854-1200C>T	rs35386923	0.53647
NM_152783.5(D2HGDH):c.1276G>A (p.Ala426Thr)	rs146578303	0.00633

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