List of variants in gene MT-ND1 reported as likely 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: 23

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ND1):m.3340C>T	rs1603218910
NC_012920.1(MT-ND1):m.3344T>C	rs1603218912
NC_012920.1(MT-ND1):m.3368T>C	rs1603218920
NC_012920.1(MT-ND1):m.3385A>G	rs879050714
NC_012920.1(MT-ND1):m.3395A>G	rs1556422722
NC_012920.1(MT-ND1):m.3492A>C	rs878950749
NC_012920.1(MT-ND1):m.3533C>T	rs377091327
NC_012920.1(MT-ND1):m.3535T>A	rs1603219004
NC_012920.1(MT-ND1):m.3628A>T	rs1603219051
NC_012920.1(MT-ND1):m.3640G>A	rs1603219059
NC_012920.1(MT-ND1):m.3644T>C	rs878991470
NC_012920.1(MT-ND1):m.3808A>G	rs2854135
NC_012920.1(MT-ND1):m.3943A>G	rs879176055
NC_012920.1(MT-ND1):m.4029C>A	rs1603219264
NC_012920.1(MT-ND1):m.4058C>T	rs1603219282
NC_012920.1(MT-ND1):m.4084G>A	rs1603219293
NC_012920.1(MT-ND1):m.4132G>A	rs1057520201
NC_012920.1(MT-ND1):m.4205T>C	rs1603219353
NC_012920.1(MT-ND1):m.4226T>C	rs1603219365
NC_012920.1(MT-ND1):m.4231A>G	rs878929819
NC_012920.1(MT-ND1):m.4234A>G	rs1603219368
NC_012920.1(MT-ND1):m.4243A>G	rs1603219373
m.3308T>G	rs28358582

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