ClinVar Miner

Submissions for variant NM_000523.4(HOXD13):c.135C>T (p.Ser45=)

gnomAD frequency: 0.00029  dbSNP: rs757175860
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000344768 SCV000340137 uncertain significance not provided 2018-05-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000344768 SCV004370600 benign not provided 2023-11-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000344768 SCV005188064 uncertain significance not provided criteria provided, single submitter not provided

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