List of variants in gene TET3 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001287491.2(TET3):c.2536T>C (p.Leu846=)	rs7560668	0.39767
NM_001287491.2(TET3):c.4524G>C (p.Leu1508=)	rs60481444	0.05465
NM_001287491.2(TET3):c.1285C>T (p.Pro429Ser)	rs61741171	0.04165
NM_001287491.2(TET3):c.5172G>A (p.Gln1724=)	rs79170439	0.02799
NM_001287491.2(TET3):c.4959C>T (p.Gly1653=)	rs116688476	0.01923
NM_001287491.2(TET3):c.1371C>T (p.Pro457=)	rs61742889	0.01009
NM_001287491.2(TET3):c.1700T>C (p.Val567Ala)	rs148646838	0.00702
NM_001287491.2(TET3):c.360+47G>A	rs185515634	0.00469
NM_001287491.2(TET3):c.1934C>T (p.Pro645Leu)	rs201583228	0.00447
NM_001287491.2(TET3):c.2805C>T (p.Leu935=)	rs115293949	0.00329
NM_001287491.2(TET3):c.2135G>A (p.Arg712Gln)	rs57955681	0.00188
NM_001287491.2(TET3):c.4881C>T (p.Gly1627=)
NM_001287491.2(TET3):c.5151G>A (p.Ala1717=)

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