Variants in gene DTNA with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001386795.1(DTNA):c.1297C>T (p.His433Tyr)	rs139872140	0.00207
NM_001386795.1(DTNA):c.1000G>A (p.Val334Met)	rs148123045	0.00120
NM_001386795.1(DTNA):c.955A>G (p.Met319Val)	rs141981161	0.00047
NM_001386795.1(DTNA):c.1480G>A (p.Asp494Asn)	rs144880521	0.00037
NM_001386795.1(DTNA):c.2039G>A (p.Arg680Gln)	rs138143719	0.00034
NM_001386795.1(DTNA):c.2108G>A (p.Arg703Gln)	rs142009291	0.00028
NM_001386795.1(DTNA):c.1086-321A>C	rs191973037	0.00010
NM_001386795.1(DTNA):c.1838C>T (p.Pro613Leu)	rs145425478	0.00003
NM_001386795.1(DTNA):c.68-7G>A	rs372126412	0.00003
NM_001386795.1(DTNA):c.1695C>T (p.Ser565=)	rs774966330	0.00001
NM_001386795.1(DTNA):c.2224G>T (p.Val742Phe)	rs533568822	0.00001
NM_001386795.1(DTNA):c.476G>A (p.Ser159Asn)	rs147115867	0.00001
NM_001386795.1(DTNA):c.68-5A>G	rs1243110074	0.00001
NM_001386795.1(DTNA):c.1766G>A (p.Arg589His)	rs200246467

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