ClinVar Miner

Variants with conflicting interpretations "benign" from Center for Advanced Laboratory Medicine, UC San Diego Health, University of California San Diego and "uncertain significance" from any submitter

Minimum review status of the submission from Center for Advanced Laboratory Medicine, UC San Diego Health, University of California San Diego: Collection method of the submission from Center for Advanced Laboratory Medicine, UC San Diego Health, University of California San Diego:
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_001943.5(DSG2):c.2759T>G (p.Val920Gly) rs142841727 0.00439
NM_144573.4(NEXN):c.995A>C (p.Glu332Ala) rs201763096 0.00262
NM_001134363.3(RBM20):c.448G>A (p.Ala150Thr) rs199868951 0.00055

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