List of variants in gene AGPS reported as benign for peroxisomal disease

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: 34

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HGVS	dbSNP	gnomAD frequency
NM_003659.4(AGPS):c.1362+79G>A	rs12468046	0.87026
NM_003659.4(AGPS):c.442-64C>T	rs3754989	0.85863
NM_003659.4(AGPS):c.*1866A>G	rs10930795	0.83889
NM_003659.4(AGPS):c.*4253C>A	rs10803912	0.83746
NM_003659.4(AGPS):c.*4974T>C	rs2293475	0.83675
NM_003659.4(AGPS):c.*3558C>T	rs8941	0.72163
NM_003659.4(AGPS):c.1608-95T>A	rs2364854	0.57249
NM_003659.4(AGPS):c.4516_4517del	rs3215354	0.11154
NM_003659.4(AGPS):c.1856-16G>T	rs3213945	0.08514
NM_003659.4(AGPS):c.*4821C>T	rs28576781	0.03281
NM_003659.4(AGPS):c.207A>G (p.Ala69=)	rs34744592	0.02410
NM_003659.4(AGPS):c.*2636G>C	rs77450843	0.02159
NM_003659.4(AGPS):c.*4618A>G	rs75827012	0.02017
NM_003659.4(AGPS):c.261-5A>C	rs73029113	0.01813
NM_003659.4(AGPS):c.*552T>G	rs115060780	0.01756
NM_003659.4(AGPS):c.*1106A>T	rs116688077	0.01515
NM_003659.4(AGPS):c.1173C>G (p.Gly391=)	rs115580413	0.01496
NM_003659.4(AGPS):c.1704G>A (p.Thr568=)	rs36052691	0.00710
NM_003659.4(AGPS):c.*3894A>G	rs74988186	0.00708
NM_003659.4(AGPS):c.*1719G>A	rs182366015	0.00706
NM_003659.4(AGPS):c.*1364A>G	rs144780787	0.00608
NM_003659.4(AGPS):c.*4098C>T	rs115549933	0.00496
NM_003659.4(AGPS):c.*2091T>C	rs16865338	0.00368
NM_003659.4(AGPS):c.*2548A>G	rs76966937	0.00233
NM_003659.4(AGPS):c.1233+5A>G	rs370777451	0.00181
NM_003659.4(AGPS):c.*3045C>T	rs147676340	0.00071
NM_003659.4(AGPS):c.*865A>G	rs2293470	0.00066
NM_003659.4(AGPS):c.1814_1815insAGAA	rs61052002
NM_003659.4(AGPS):c.*1880AT[8]	rs59535792
NM_003659.4(AGPS):c.*377C>G	rs112754713
NM_003659.4(AGPS):c.*377C>T	rs112754713
NM_003659.4(AGPS):c.*3854dup	rs397783598
NM_003659.4(AGPS):c.1152C>A (p.Val384=)	rs529236041
NM_003659.4(AGPS):c.563-10del	rs3834134

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