ClinVar Miner

Variants with conflicting interpretations "pathogenic" from Medgenome Labs Pvt Ltd and "likely pathogenic" from any submitter

Minimum review status of the submission from Medgenome Labs Pvt Ltd: Collection method of the submission from Medgenome Labs Pvt Ltd:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 3
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HGVS dbSNP gnomAD frequency
NM_024339.5(THOC6):c.298T>A (p.Trp100Arg) rs138632121 0.00020
NM_024339.5(THOC6):c.824G>A (p.Gly275Asp) rs200426926 0.00020
NM_031296.3(RAB33B):c.186del (p.Glu63fs) rs1561002040

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