ClinVar Miner

Submissions for variant GRCh37/hg19 13q33.1(chr13:102250764-102412039)x1

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics of Human Eye Development, Oxford Brookes University RCV003134417 SCV002570104 pathogenic Spinocerebellar ataxia type 27 2022-08-25 criteria provided, single submitter research

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