ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.536-80C>T

gnomAD frequency: 0.00112  dbSNP: rs137869443
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breakthrough Genomics, Breakthrough Genomics RCV004706070 SCV005217346 likely benign not provided criteria provided, single submitter not provided
Leiden Open Variation Database RCV001194831 SCV001364639 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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