ClinVar Miner

Submissions for variant NC_000023.11:g.101398823_101398824ins(300)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centogene AG - the Rare Disease Company RCV001251113 SCV001426477 pathogenic Fabry disease criteria provided, single submitter clinical testing

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