List of variants in gene OGDH reported as benign by Mayo Clinic Laboratories, Mayo Clinic

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_002541.4(OGDH):c.2973G>A (p.Ala991=)	rs2070606	0.13683
NM_002541.4(OGDH):c.3052G>A (p.Val1018Ile)	rs2070607	0.03912
NM_002541.4(OGDH):c.345A>G (p.Glu115=)	rs11557280	0.03827
NM_002541.4(OGDH):c.2988C>T (p.Thr996=)	rs61756583	0.03821
NM_002541.4(OGDH):c.3063C>T (p.Asn1021=)	rs61756584	0.03755
NM_002541.4(OGDH):c.396G>A (p.Ser132=)	rs41280648	0.03200
NM_002541.4(OGDH):c.2784A>G (p.Thr928=)	rs112309751	0.00894

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