ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.1683+20C>T

dbSNP: rs776626195
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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 RCV001864189 SCV002125534 uncertain significance Fanconi anemia 2021-11-28 criteria provided, single submitter clinical testing In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may create or strengthen a splice site. This variant has not been reported in the literature in individuals affected with SLX4-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change falls in intron 7 of the SLX4 gene. It does not directly change the encoded amino acid sequence of the SLX4 protein.

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