List of variants in gene DTNA reported as 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001386795.1(DTNA):c.1743+14G>A	rs1617318	0.37431
NM_001386795.1(DTNA):c.1903+8G>A	rs111817603	0.01438
NM_001386795.1(DTNA):c.1821G>A (p.Ala607=)	rs9959365	0.00984
NM_001386795.1(DTNA):c.537G>T (p.Thr179=)	rs11877640	0.00956
NM_001386795.1(DTNA):c.933C>T (p.Ser311=)	rs114170541	0.00902
NM_001386795.1(DTNA):c.2162+14G>A	rs76713874	0.00820
NM_001386795.1(DTNA):c.1438C>A (p.Pro480Thr)	rs77320474	0.00593
NM_001386795.1(DTNA):c.210G>A (p.Leu70=)	rs117571555	0.00459
NM_001386795.1(DTNA):c.1993+7T>C	rs138590000	0.00403
NM_001386795.1(DTNA):c.243A>G (p.Leu81=)	rs146923532	0.00285
NM_001386795.1(DTNA):c.999C>T (p.Ile333=)	rs61737438	0.00258
NM_001386795.1(DTNA):c.604-14G>T	rs397517447	0.00123
NM_001386795.1(DTNA):c.1875G>A (p.Gly625=)	rs542483546	0.00004
NM_001386795.1(DTNA):c.231C>T (p.Asn77=)	rs147759402

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