ClinVar Miner

Submissions for variant NM_017583.6(TRIM44):c.670-27G>C

gnomAD frequency: 0.13698  dbSNP: rs3740798
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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 RCV001838946 SCV002098735 benign Aniridia 3 2021-09-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004718988 SCV005316130 benign not provided criteria provided, single submitter not provided

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