ClinVar Miner

Submissions for variant NM_014874.4(MFN2):c.*221_*222dup

dbSNP: rs558848411
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000317896 SCV000348020 likely benign Hereditary motor and sensory neuropathy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000372531 SCV000348021 likely benign Charcot-Marie-Tooth disease type 2 2016-06-14 criteria provided, single submitter clinical testing

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