ClinVar Miner

Submissions for variant NM_033100.4(CDHR1):c.476C>A (p.Ala159Glu) (rs763399323)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Developmental Genetics Unit,King Faisal Specialist Hospital & Research Centre RCV000171179 SCV000221376 likely pathogenic not provided no assertion criteria provided research

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