List of variants in gene MT-ND4L reported as uncertain significance 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: 12

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ND4L):m.10489A>G	rs1603222854
NC_012920.1(MT-ND4L):m.10492T>C	rs1603222857
NC_012920.1(MT-ND4L):m.10522G>A	rs1603222873
NC_012920.1(MT-ND4L):m.10524A>G	rs1603222875
NC_012920.1(MT-ND4L):m.10579T>C	rs1603222900
NC_012920.1(MT-ND4L):m.10600C>T	rs1603222912
NC_012920.1(MT-ND4L):m.10602A>G	rs1603222913
NC_012920.1(MT-ND4L):m.10620A>G	rs1603222915
NC_012920.1(MT-ND4L):m.10630T>C	rs1603222919
NC_012920.1(MT-ND4L):m.10677G>A	rs1603222944
NC_012920.1(MT-ND4L):m.10686G>A	rs1603222946
NC_012920.1(MT-ND4L):m.10749A>G	rs1603222963

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