Variants in gene DTNA 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001386795.1(DTNA):c.2162+14G>A	rs76713874	0.00820
NM_001386795.1(DTNA):c.210G>A (p.Leu70=)	rs117571555	0.00459
NM_001386795.1(DTNA):c.1435-19T>C	rs141620769	0.00328
NM_001386795.1(DTNA):c.243A>G (p.Leu81=)	rs146923532	0.00285
NM_001386795.1(DTNA):c.1176-8T>C	rs41274310	0.00216
NM_001386795.1(DTNA):c.1297C>T (p.His433Tyr)	rs139872140	0.00207
NM_001386795.1(DTNA):c.604-14G>T	rs397517447	0.00123
NM_001386795.1(DTNA):c.1000G>A (p.Val334Met)	rs148123045	0.00120
NM_001386795.1(DTNA):c.2178A>C (p.Ala726=)	rs145486636	0.00063
NM_001386795.1(DTNA):c.1485G>A (p.Ala495=)	rs397517443	0.00016
NM_001386795.1(DTNA):c.1454G>C (p.Ser485Thr)	rs190619495	0.00008
NM_001386795.1(DTNA):c.603+15T>C	rs367772080	0.00006
NM_001386795.1(DTNA):c.675G>A (p.Leu225=)	rs376519672	0.00005
NM_001386795.1(DTNA):c.1875G>A (p.Gly625=)	rs542483546	0.00004
NM_001386795.1(DTNA):c.1744-10G>A	rs192561043
NM_001386795.1(DTNA):c.1744-10G>T	rs192561043

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