ClinVar Miner

Submissions for variant NM_000522.5(HOXA13):c.234T>A (p.Ala78=)

dbSNP: rs1308135144
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000910589 SCV001055461 likely benign not provided 2018-02-01 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002505334 SCV002805017 likely benign Guttmacher syndrome; Hand-foot-genital syndrome 2021-07-26 criteria provided, single submitter clinical testing

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