Variants in gene combination DNAAF3, TNNI3 with conflicting interpretations reported as "likely benign and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001256715.2(DNAAF3):c.1239-8A>G	rs28377509	0.36480
NM_000363.5(TNNI3):c.25-8T>A	rs3729836	0.35138
NM_001256715.2(DNAAF3):c.1056G>A (p.Pro352=)	rs891187	0.29351
NM_001256715.2(DNAAF3):c.666T>C (p.Ala222=)	rs7260320	0.27290
NM_001256715.2(DNAAF3):c.875A>G (p.Glu292Gly)	rs2365725	0.24847
NM_001256715.2(DNAAF3):c.790-14C>T	rs7260371	0.24759
NM_000363.5(TNNI3):c.-35C>A	rs3729707	0.07367
NM_000363.5(TNNI3):c.150+13G>A	rs73617692	0.07353
NM_001256715.2(DNAAF3):c.1164-14C>T	rs60176657	0.06188
NM_001256715.2(DNAAF3):c.510A>G (p.Val170=)	rs56726774	0.06016
NM_001256715.2(DNAAF3):c.327A>G (p.Arg109=)	rs3848618	0.05626
NM_001256715.2(DNAAF3):c.529G>A (p.Gly177Ser)	rs58824375	0.05620
NM_000363.5(TNNI3):c.204G>T (p.Arg68=)	rs3729711	0.04033
NM_001256715.2(DNAAF3):c.1248G>A (p.Val416=)	rs111250144	0.00398
NM_001256715.2(DNAAF3):c.531C>T (p.Gly177=)	rs559008223	0.00192
NM_001256715.2(DNAAF3):c.1093= (p.Asn365=)	rs890872

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