List of variants in gene DTNA reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 18

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HGVS	dbSNP	gnomAD frequency
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.2178A>C (p.Ala726=)	rs145486636	0.00063
NM_001386795.1(DTNA):c.955A>G (p.Met319Val)	rs141981161	0.00047
NM_001386795.1(DTNA):c.51G>A (p.Gln17=)	rs368000651	0.00030
NM_001386795.1(DTNA):c.2108G>A (p.Arg703Gln)	rs142009291	0.00028
NM_001386795.1(DTNA):c.126G>A (p.Arg42=)	rs376001633	0.00020
NM_001386795.1(DTNA):c.1485G>A (p.Ala495=)	rs397517443	0.00016
NM_001386795.1(DTNA):c.603+15T>C	rs367772080	0.00006
NM_001386795.1(DTNA):c.1491G>A (p.Lys497=)	rs397517444	0.00001
NM_001386795.1(DTNA):c.228C>T (p.Leu76=)	rs1002773493	0.00001
NM_001386795.1(DTNA):c.67+12T>A	rs876657460	0.00001
NM_001386795.1(DTNA):c.148+7A>G	rs397517445
NM_001386795.1(DTNA):c.1744-10G>A	rs192561043
NM_001386795.1(DTNA):c.1744-10G>T	rs192561043
NM_001386795.1(DTNA):c.1770C>A (p.Ser590=)	rs570093404
NM_001386795.1(DTNA):c.189G>A (p.Arg63=)	rs727505106
NM_001386795.1(DTNA):c.1971T>G (p.Ser657=)	rs199855849

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