List of variants in gene TNC reported as benign by Athena Diagnostics Inc

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_002160.4(TNC):c.5341G>A (p.Ala1781Thr)	rs2274750	0.05620
NM_002160.4(TNC):c.2389A>C (p.Arg797=)	rs16932195	0.03496
NM_002160.4(TNC):c.2562C>T (p.Asp854=)	rs61739209	0.02872
NM_002160.4(TNC):c.1813G>A (p.Val605Ile)	rs3827816	0.02047
NM_002160.4(TNC):c.5193G>A (p.Arg1731=)	rs61265377	0.01721
NM_002160.4(TNC):c.6144G>A (p.Gly2048=)	rs79563958	0.01419
NM_002160.4(TNC):c.3165C>T (p.Ala1055=)	rs3748172	0.01315
NM_002160.4(TNC):c.2620A>G (p.Ile874Val)	rs61737743	0.01101
NM_002160.4(TNC):c.781G>A (p.Gly261Ser)	rs61736826	0.01088
NM_002160.4(TNC):c.1642G>A (p.Val548Met)	rs61729478	0.00984
NM_002160.4(TNC):c.1719C>T (p.Cys573=)	rs141544394	0.00347
NM_002160.4(TNC):c.945C>T (p.Cys315=)	rs148465701	0.00226
NM_002160.4(TNC):c.628G>A (p.Gly210Ser)	rs144032672	0.00159
NM_002160.4(TNC):c.2374G>T (p.Gly792Cys)	rs150868783	0.00131
NM_002160.4(TNC):c.61G>A (p.Glu21Lys)	rs141126037	0.00125
NM_002160.4(TNC):c.5093G>A (p.Arg1698Gln)	rs61734387
NM_002160.4(TNC):c.6099C>T (p.Arg2033=)	rs58547879

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