ClinVar Miner

Submissions for variant NM_014874.3(MFN2):c.1709A>G (p.Asn570Ser) (rs376925978)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Inherited Neuropathy Consortium RCV000790315 SCV000929723 uncertain significance Charcot-Marie-Tooth disease no assertion criteria provided literature only
Genesis Genome Database RCV000790315 SCV000999683 uncertain significance Charcot-Marie-Tooth disease 2019-08-14 no assertion criteria provided research

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