ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.3903G>T (p.Gly1301=)

dbSNP: rs753464234
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001341575 SCV001535455 likely benign Fanconi anemia 2024-03-04 criteria provided, single submitter clinical testing

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