ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.4739+24G>T

gnomAD frequency: 0.09148  dbSNP: rs12933120
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001644945 SCV001860449 benign not provided 2019-01-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001644945 SCV005293912 benign not provided criteria provided, single submitter not provided
Leiden Open Variation Database RCV001194862 SCV001364699 likely benign not specified 2012-08-31 no assertion criteria provided curation Curator: Arleen D. Auerbach. Submitter to LOVD: Janine Bakker.

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