List of variants in gene UGDH reported as likely pathogenic for epilepsy

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

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_003359.4(UGDH):c.193C>T (p.Arg65Ter)	rs200059198	0.00012
NM_003359.4(UGDH):c.950G>A (p.Arg317Gln)	rs775162839	0.00006
NM_003359.4(UGDH):c.131C>T (p.Ala44Val)	rs749975104	0.00004
NM_003359.4(UGDH):c.1177C>T (p.Arg393Trp)	rs113094436	0.00002
NM_003359.4(UGDH):c.528_531del (p.Asp176fs)

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