ClinVar Miner

List of variants reported as pathogenic for syndrome caused by partial chromosomal deletion by Knight Diagnostic Laboratories, Oregon Health and Sciences University

Included ClinVar conditions (110):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_006940.6(SOX5):c.1711C>T (p.Arg571Trp) rs1565669640

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