ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.2898G>A (p.Gln966=)

gnomAD frequency: 0.00006  dbSNP: rs748700450
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000865434 SCV001006395 likely benign Fanconi anemia 2024-11-15 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002501245 SCV002812458 likely benign Fanconi anemia complementation group P 2021-10-27 criteria provided, single submitter clinical testing

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