ClinVar Miner

Submissions for variant NM_020223.4(FAM20C):c.1506-55G>A

dbSNP: rs36156024
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001544311 SCV001763324 benign Lethal osteosclerotic bone dysplasia 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001598693 SCV001827542 benign not provided 2021-03-28 criteria provided, single submitter clinical testing

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