ClinVar Miner

List of variants reported as uncertain significance for Hearing impairment; Microcephaly; Developmental delay; Congenital cardiomyopathy

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Total variants: 3
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HGVS dbSNP gnomAD frequency
NC_012920.1:m.12013A>G rs1057516067
NC_012920.1:m.12018C>G rs1057516068
NC_012920.1:m.13713C>A rs879193643

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