ClinVar Miner

Submissions for variant NM_000112.4(SLC26A2):c.105A>G (p.Ser35=)

dbSNP: rs765269781
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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 RCV001413637 SCV001615756 likely benign Achondrogenesis, type IB; Atelosteogenesis type II; Multiple epiphyseal dysplasia type 4; Diastrophic dysplasia 2024-10-28 criteria provided, single submitter clinical testing

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