ClinVar Miner

Submissions for variant NM_018972.4(GDAP1):c.802_803del (p.Trp268fs) (rs765346218)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Kariminejad - Najmabadi Pathology & Genetics Center RCV001007464 SCV001167076 uncertain significance Charcot-Marie-Tooth disease type 2K criteria provided, single submitter clinical testing

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