ClinVar Miner

Submissions for variant NM_006297.3(XRCC1):c.1481+9G>A

gnomAD frequency: 0.37650  dbSNP: rs25479
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001651867 SCV001862334 benign not provided 2019-07-01 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243358 SCV002514030 benign Spinocerebellar ataxia, autosomal recessive 26 2021-12-05 criteria provided, single submitter clinical testing

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