List of variants in gene AGBL3 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_178563.4(AGBL3):c.1655C>T (p.Thr552Met)	rs117168663	0.00860
NM_178563.4(AGBL3):c.612C>T (p.His204=)	rs74319573	0.00660
NM_178563.4(AGBL3):c.154C>T (p.Arg52Trp)	rs186048202	0.00635
NM_178563.4(AGBL3):c.208C>T (p.Arg70Cys)	rs117732894	0.00631
NM_178563.4(AGBL3):c.1995G>A (p.Gly665=)	rs190310134	0.00250
NM_178563.4(AGBL3):c.131C>G (p.Ser44Cys)	rs148391971	0.00246

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