ClinVar Miner

Submissions for variant NM_006492.3(ALX3):c.627G>A (p.Arg209=)

gnomAD frequency: 0.00190  dbSNP: rs113851340
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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 RCV000253012 SCV000311498 likely benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000911637 SCV001056711 benign not provided 2024-08-29 criteria provided, single submitter clinical testing

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