ClinVar Miner

List of variants in gene MT-ND4 reported as likely benign for Leigh syndrome

Included ClinVar conditions (11):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
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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