ClinVar Miner

Submissions for variant NM_000522.5(HOXA13):c.407C>A (p.Ser136Ter)

dbSNP: rs1158254994
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000016019 SCV000036286 pathogenic Hand-foot-genital syndrome 2000-07-01 no assertion criteria provided literature only

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