ClinVar Miner

Submissions for variant NM_022166.4(XYLT1):c.2535G>C (p.Ser845=)

dbSNP: rs746392043
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001443376 SCV001646346 likely benign Desbuquois dysplasia 1 2021-03-18 criteria provided, single submitter clinical testing

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