ClinVar Miner

Submissions for variant NM_000090.4(COL3A1):c.3364-3C>T

dbSNP: rs2153503944
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001574035 SCV001800748 likely benign not provided no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001574035 SCV001808188 likely benign not provided no assertion criteria provided clinical testing

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