ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.2013+137G>C

gnomAD frequency: 0.07384  dbSNP: rs80186343
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001709710 SCV001938179 benign not provided 2019-02-24 criteria provided, single submitter clinical testing
Leiden Open Variation Database RCV001194820 SCV001364623 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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