ClinVar Miner

List of variants in gene MT-TT reported as likely benign for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP
NC_012920.1(MT-CYB):m.15893T>C rs1603225570
NC_012920.1(MT-CYB):m.15895T>C rs1603225571
NC_012920.1(MT-CYB):m.15909A>G rs1556424690
NC_012920.1(MT-CYB):m.15911A>G rs1603225583
NC_012920.1(MT-CYB):m.15925C>T rs1603225595
NC_012920.1(MT-CYB):m.15936A>G rs1556424701
NC_012920.1(MT-CYB):m.15937A>T rs1603225605
NC_012920.1(MT-CYB):m.15937del rs1603225604
NC_012920.1(MT-CYB):m.15944T>C rs1603225608
NC_012920.1(MT-CYB):m.15952C>T rs1603225613

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