ClinVar Miner

Submissions for variant NM_000090.4(COL3A1):c.753del (p.Gly252fs)

dbSNP: rs2153501973
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 Diagnostics Laboratory, Amsterdam University Medical Center RCV001579563 SCV001807702 pathogenic not provided no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001579563 SCV001930495 pathogenic not provided no assertion criteria provided clinical testing

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