ClinVar Miner

Submissions for variant NM_173596.3(SLC39A5):c.-14T>C

gnomAD frequency: 0.99669  dbSNP: rs1274497
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001807825 SCV002057004 benign Myopia 24, autosomal dominant 2021-07-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004707731 SCV005233063 benign not provided criteria provided, single submitter not provided

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