List of variants in gene combination LOC129935473, NDUFS1 reported as uncertain significance 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_005006.7(NDUFS1):c.-75A>G	rs138818421	0.00612
NM_005006.7(NDUFS1):c.-61G>C	rs367762150	0.00003
NM_005006.6(NDUFS1):c.-149T>G	rs572965960
NM_005006.7(NDUFS1):c.-101G>A	rs983757976
NM_005006.7(NDUFS1):c.-31A>G	rs1687818178
NM_005006.7(NDUFS1):c.-38T>G	rs1559071008
NM_005006.7(NDUFS1):c.-73C>A	rs367649369

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