List of variants in gene TRDN reported as benign for Cardiovascular phenotype

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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: 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.1188A>G (p.Lys396=)	rs6901953	0.35392
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.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.403G>A (p.Glu135Lys)	rs192289289	0.00900
NM_006073.4(TRDN):c.274G>A (p.Val92Ile)	rs34808221	0.00711
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.932-4C>G	rs77768246	0.00098
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.497AAAAAG[1] (p.166EK[1])	rs148596612

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