ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.2854_2855delinsAT (p.Ala952Met)

dbSNP: rs863224277
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000199487 SCV000252879 benign Fanconi anemia 2024-02-01 criteria provided, single submitter clinical testing
Vantari Genetics RCV000210791 SCV000267091 likely benign Hereditary cancer-predisposing syndrome 2015-12-07 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316099 SCV004015464 benign Fanconi anemia complementation group P 2023-07-07 criteria provided, single submitter clinical testing
Leiden Open Variation Database RCV001194836 SCV001364652 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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