ClinVar Miner

List of variants reported as pathogenic for bone neoplasm by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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_024529.5(CDC73):c.271C>T (p.Arg91Ter) rs1558280170

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