ClinVar Miner

Variants with conflicting interpretations "uncertain significance" from Clinical Genomics Laboratory, Washington University in St. Louis and "likely pathogenic" from any submitter

Minimum review status of the submission from Clinical Genomics Laboratory, Washington University in St. Louis: Collection method of the submission from Clinical Genomics Laboratory, Washington University in St. Louis:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 2
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HGVS dbSNP gnomAD frequency
NM_001042492.3(NF1):c.2117C>T (p.Ala706Val) rs2151425819
NM_001378974.1(FBXW11):c.1150C>T (p.Arg384Trp) rs1758081729

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