ClinVar Miner

Submissions for variant NC_000009.12:g.134824601del

dbSNP: rs1588597744
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
Mendelics RCV000988286 SCV001137951 pathogenic Ehlers-Danlos syndrome, classic type 2019-05-28 criteria provided, single submitter clinical testing

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