ClinVar Miner

Submissions for variant NM_000522.5(HOXA13):c.421_422insAGGCGGGCC (p.Gly140_Pro141insGlnAlaGly)

dbSNP: rs35599078
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000723201 SCV003244502 benign not provided 2024-01-15 criteria provided, single submitter clinical testing
Gharavi Laboratory, Columbia University RCV000723201 SCV000854332 uncertain significance not provided 2018-09-16 no assertion criteria provided research

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