ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.1683+9C>T

dbSNP: rs1242929879
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002172156 SCV002334351 likely benign Fanconi anemia 2021-06-19 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494035 SCV002798118 likely benign Fanconi anemia complementation group P 2022-03-08 criteria provided, single submitter clinical testing

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