List of variants in gene DLD reported as benign for Leigh syndrome

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_000108.5(DLD):c.*487C>T	rs4518	0.66588
NM_000108.5(DLD):c.*978T>C	rs2158835	0.66205
NM_000108.5(DLD):c.*1451T>C	rs2108223	0.66202
NM_000108.5(DLD):c.439-7T>C	rs10263341	0.65991
NM_000108.5(DLD):c.*207G>A	rs4564	0.65906
NM_000108.5(DLD):c.*947G>T	rs7777259	0.38028
NM_000108.5(DLD):c.*18A>T	rs8721	0.31523
NM_000108.5(DLD):c.*1688G>A	rs8440	0.31157
NM_000108.5(DLD):c.*28G>T	rs17154615	0.11990
NM_000108.5(DLD):c.684+7G>A	rs75123588	0.06110
NM_000108.5(DLD):c.1351C>T (p.Leu451=)	rs1803921	0.04354
NM_000108.5(DLD):c.685-14T>A	rs80111449	0.02638
NM_000108.5(DLD):c.*855C>T	rs116055514	0.01464
NM_000108.5(DLD):c.*648G>A	rs57801571	0.00985
NM_000108.5(DLD):c.*1300A>G	rs77095705	0.00939
NM_000108.5(DLD):c.249T>C (p.Val83=)	rs2228664	0.00921
NM_000108.5(DLD):c.777A>G (p.Lys259=)	rs1065762	0.00882
NM_000108.5(DLD):c.*1074C>G	rs149275540	0.00531
NM_000108.5(DLD):c.*470G>T	rs111619940

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