ClinVar Miner

Submissions for variant NM_013382.7(POMT2):c.1116+35A>G

gnomAD frequency: 0.01815  dbSNP: rs2302831
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000243326 SCV000311974 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001567856 SCV001791620 likely benign not provided 2018-07-15 criteria provided, single submitter clinical testing

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