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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