ClinVar Miner

List of variants in gene AGPS reported as benign for bone disorder

Included ClinVar conditions (1346):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
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.*4253C>A rs10803912 0.83746
NM_003659.4(AGPS):c.*4974T>C rs2293475 0.83675
NM_003659.4(AGPS):c.*1866A>G rs10930795 0.82837
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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