List of variants in gene TRDN reported as benign by PreventionGenetics, part of Exact Sciences

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_006073.4(TRDN):c.601C>G (p.Leu201Val)	rs6902416	0.84721
NM_006073.4(TRDN):c.383C>G (p.Thr128Ser)	rs9490809	0.50546
NM_006073.4(TRDN):c.2051-19G>A	rs7754205	0.42872
NM_006073.4(TRDN):c.1188A>G (p.Lys396=)	rs6901953	0.35392
NM_006073.4(TRDN):c.1186+16C>T	rs3813328	0.33405
NM_006073.4(TRDN):c.1257C>A (p.Asp419Glu)	rs17737379	0.17356
NM_006073.4(TRDN):c.1370-11C>A	rs9401658	0.16989
NM_006073.4(TRDN):c.1211T>G (p.Val404Gly)	rs28494009	0.16504
NM_006073.4(TRDN):c.1408C>A (p.Leu470Met)	rs6569336	0.09024
NM_006073.4(TRDN):c.1105+5G>A	rs41284430	0.03253
NM_006073.4(TRDN):c.1620A>G (p.Ile540Met)	rs7771303	0.01556
NM_006073.4(TRDN):c.1096G>A (p.Ala366Thr)	rs35047281	0.01253
NM_006073.4(TRDN):c.1016G>A (p.Ser339Asn)	rs35766971	0.01214
NM_006073.4(TRDN):c.430C>T (p.His144Tyr)	rs79182520	0.00232
NM_006073.4(TRDN):c.1313T>A (p.Ile438Asn)	rs2873479
NM_006073.4(TRDN):c.1313T>G (p.Ile438Ser)	rs2873479
NM_006073.4(TRDN):c.1598-6dup	rs147062785
NM_006073.4(TRDN):c.497AAAAAG[1] (p.166EK[1])	rs148596612

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