List of variants in gene combination NPHP3-ACAD11, UBA5 reported as benign for not provided

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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_024818.6(UBA5):c.1024+32T>C	rs2305629	0.41651
NM_024818.6(UBA5):c.1131+17A>T	rs12635575	0.23542
NM_024818.6(UBA5):c.683C>T (p.Ala228Val)	rs35064843	0.01657
NM_024818.6(UBA5):c.939G>A (p.Glu313=)	rs111904472	0.00121
NM_024818.6(UBA5):c.812+20del

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