ClinVar Miner

Submissions for variant NM_000523.4(HOXD13):c.41C>T (p.Ala14Val)

gnomAD frequency: 0.00891  dbSNP: rs555136684
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000290295 SCV000333830 benign not specified 2017-04-12 criteria provided, single submitter clinical testing
GeneDx RCV000865396 SCV000532942 likely benign not provided 2021-02-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000865396 SCV001006351 benign not provided 2024-11-27 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000865396 SCV005257099 likely benign not provided criteria provided, single submitter not provided

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