ClinVar Miner

Submissions for variant NM_001005273.3(CHD3):c.385-56C>G

dbSNP: rs12450454
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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 RCV001579013 SCV001806401 benign Snijders Blok-Campeau syndrome 2021-07-22 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004710327 SCV005251548 benign not provided criteria provided, single submitter not provided

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