ClinVar Miner

Variants with conflicting interpretations "pathogenic" from Samuels research lab, Centre de Recherche du CHU Ste-Justine and "uncertain significance" from any submitter

Minimum review status of the submission from Samuels research lab, Centre de Recherche du CHU Ste-Justine: Collection method of the submission from Samuels research lab, Centre de Recherche du CHU Ste-Justine:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 1
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HGVS dbSNP gnomAD frequency
NM_001322934.2(NFKB2):c.2600C>T (p.Ala867Val) rs727502788

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