ClinVar Miner

Submissions for variant NM_003244.4(TGIF1):c.16+1805del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Wuerzburg RCV003881687 SCV004697364 likely pathogenic Holoprosencephaly 4 no assertion criteria provided clinical testing

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