ClinVar Miner

Submissions for variant NM_020297.4(ABCC9):c.2020-6T>C

dbSNP: rs1234670723
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics, Academic Medical Center RCV001700911 SCV001925996 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001702979 SCV001930477 likely benign not provided no assertion criteria provided clinical testing

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