ClinVar Miner

Submissions for variant NM_020297.4(ABCC9):c.1011+100dup

dbSNP: rs3835048
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001548917 SCV001768925 benign Hypertrichotic osteochondrodysplasia Cantu type 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001694088 SCV001910287 benign not provided 2018-06-14 criteria provided, single submitter clinical testing

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