ClinVar Miner

List of variants in gene NDUFB11 reported as likely pathogenic by Cardiovascular Biomedical Research Unit, Royal Brompton & Harefield NHS Foundation Trust

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Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_001135998.3(NDUFB11):c.262C>T (p.Arg88Ter) rs786205225

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