ClinVar Miner

Submissions for variant NM_000523.4(HOXD13):c.183_203del (p.Ala65_Ala71del)

dbSNP: rs878854346
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000016003 SCV000036270 pathogenic Brachydactyly-syndactyly syndrome 2007-02-01 no assertion criteria provided literature only

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