ClinVar Miner

Submissions for variant NC_000008.11:g.24953635T>G

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genesis Genome Database RCV000857192 SCV000999774 uncertain significance Charcot-Marie-Tooth disease 2019-08-14 no assertion criteria provided research
Genesis Genome Database RCV000857193 SCV000999775 uncertain significance Charcot-Marie-Tooth disease, type I 2019-08-14 no assertion criteria provided research
Genesis Genome Database RCV000857194 SCV000999776 uncertain significance Autosomal dominant distal hereditary motor neuropathy 2019-08-14 no assertion criteria provided research

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