ClinVar Miner

List of variants in gene D2HGDH reported by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_152783.5(D2HGDH):c.1063G>A (p.Gly355Ser)	rs139321130	0.00949
NM_152783.5(D2HGDH):c.1276G>A (p.Ala426Thr)	rs146578303	0.00633

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