ClinVar Miner

List of variants in gene UGP2 reported as benign for Developmental and epileptic encephalopathy, 83

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_006759.4(UGP2):c.255+44G>A	rs10183479	0.82810
NM_006759.4(UGP2):c.1089G>A (p.Leu363=)	rs147051654	0.01750

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