ClinVar Miner

List of variants studied for 3-M syndrome by Cytogenetics and Molecular Genetics Section, Pathology Unit, BARC Hospital, Bhabha Atomic Research Centre

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_014780.5(CUL7):c.2943_2944del (p.Cys982fs) rs1064792895

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