Variants in gene TRDN with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 18

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HGVS	dbSNP	gnomAD frequency
NM_006073.4(TRDN):c.383C>G (p.Thr128Ser)	rs9490809	0.50546
NM_006073.4(TRDN):c.1257C>A (p.Asp419Glu)	rs17737379	0.17356
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.1620A>G (p.Ile540Met)	rs7771303	0.01556
NM_006073.4(TRDN):c.1016G>A (p.Ser339Asn)	rs35766971	0.01214
NM_006073.4(TRDN):c.403G>A (p.Glu135Lys)	rs192289289	0.00900
NM_006073.4(TRDN):c.1538-13T>G	rs55704802	0.00651
NM_006073.4(TRDN):c.1721-4A>G	rs60743141	0.00430
NM_006073.4(TRDN):c.430C>T (p.His144Tyr)	rs79182520	0.00232
NM_006073.4(TRDN):c.1531C>A (p.Pro511Thr)	rs146935076	0.00183
NM_006073.4(TRDN):c.367G>A (p.Asp123Asn)	rs201021891	0.00036
NM_006073.4(TRDN):c.1313T>A (p.Ile438Asn)	rs2873479
NM_006073.4(TRDN):c.1598-6dup	rs147062785
NM_006073.4(TRDN):c.1805-21dup	rs11373802
NM_006073.4(TRDN):c.233-14_233-13del	rs66509682
NM_006073.4(TRDN):c.497AAAAAG[1] (p.166EK[1])	rs148596612
NM_006073.4(TRDN):c.931+18del	rs201431159

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