ClinVar Miner

Submissions for variant NM_032888.4(COL27A1):c.3610-121A>G

gnomAD frequency: 0.33460  dbSNP: rs10513241
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 RCV001543910 SCV001762809 benign Steel syndrome 2021-07-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004713045 SCV005268784 benign not provided criteria provided, single submitter not provided

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