ClinVar Miner

Submissions for variant NM_002253.4(KDR):c.3848+15T>C

gnomAD frequency: 0.99680  dbSNP: rs2412617
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breakthrough Genomics, Breakthrough Genomics RCV004716588 SCV005301880 benign not provided criteria provided, single submitter not provided
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV000612206 SCV000734335 benign Capillary infantile hemangioma no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV001701117 SCV001919275 benign not specified no assertion criteria provided clinical testing

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