List of variants in gene MT-ND4 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: 20

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ND4):m.10775G>A	rs879015842
NC_012920.1(MT-ND4):m.10887A>G	rs1603223004
NC_012920.1(MT-ND4):m.10931T>C	rs1569484408
NC_012920.1(MT-ND4):m.11039C>T	rs1603223071
NC_012920.1(MT-ND4):m.11129A>G	rs1603223122
NC_012920.1(MT-ND4):m.11268C>T	rs879011423
NC_012920.1(MT-ND4):m.11318T>C	rs1603223235
NC_012920.1(MT-ND4):m.11453G>A	rs1603223293
NC_012920.1(MT-ND4):m.11582A>G	rs1603223348
NC_012920.1(MT-ND4):m.11708A>G	rs386829138
NC_012920.1(MT-ND4):m.11807A>G	rs1603223419
NC_012920.1(MT-ND4):m.11930A>G	rs1603223472
NC_012920.1(MT-ND4):m.11946C>T	rs1603223482
NC_012920.1(MT-ND4):m.11957A>G	rs1603223488
NC_012920.1(MT-ND4):m.12011T>C	rs386829144
NC_012920.1(MT-ND4):m.12014C>T	rs1603223511
NC_012920.1(MT-ND4):m.12017A>G	rs879136236
NC_012920.1(MT-ND4):m.12033A>G	rs1603223521
NC_012920.1(MT-ND4):m.12074A>C	rs1603223534
NC_012920.1(MT-ND4):m.12134T>C	rs1603223562

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