ClinVar Miner

Submissions for variant NM_181882.3(PRX):c.2612T>C (p.Val871Ala)

dbSNP: rs201389706
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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 RCV000857054 SCV000999626 uncertain significance Charcot-Marie-Tooth disease 2019-08-14 no assertion criteria provided research
Genesis Genome Database RCV000857055 SCV000999627 uncertain significance Distal spinal muscular atrophy 2019-08-14 no assertion criteria provided research
Genesis Genome Database RCV000857056 SCV000999628 uncertain significance Charcot-Marie-Tooth disease, type I 2019-08-14 no assertion criteria provided research

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