ClinVar Miner

Submissions for variant NM_005220.3(DLX3):c.853G>A (p.Ala285Thr)

gnomAD frequency: 0.00046  dbSNP: rs148713638
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000350210 SCV000335789 uncertain significance not provided 2015-10-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000350210 SCV002362927 likely benign not provided 2023-07-11 criteria provided, single submitter clinical testing

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