List of variants in gene NDUFS1 reported as benign for Leigh syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_005006.7(NDUFS1):c.*336G>T	rs1044120	0.52989
NM_005006.7(NDUFS1):c.1251A>G (p.Arg417=)	rs1801318	0.34874
NM_005006.7(NDUFS1):c.414T>C (p.Asp138=)	rs11548670	0.05713
NM_005006.7(NDUFS1):c.*733A>G	rs6707707	0.03241
NM_005006.7(NDUFS1):c.*158T>C	rs3770989	0.02543
NM_005006.7(NDUFS1):c.*399G>A	rs77000728	0.01727
NM_005006.7(NDUFS1):c.*574T>G	rs73065790	0.01005
NM_005006.7(NDUFS1):c.1393-7T>A	rs200409285	0.00018
NM_005006.7(NDUFS1):c.*457T>A	rs4147728
NM_005006.7(NDUFS1):c.*53T>G	rs116335919
NM_005006.7(NDUFS1):c.154-126TAGA[8]	rs3217140
NM_005006.7(NDUFS1):c.154-126TAGA[9]	rs3217140
NM_005006.7(NDUFS1):c.966G>T (p.Ala322=)	rs1127566

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