ClinVar Miner

Variants with conflicting interpretations "uncertain significance" from St. Jude Clinical Genomics Lab, St. Jude Children's Research Hospital and "likely benign" from CSER _CC_NCGL, University of Washington

Minimum review status of the submission from St. Jude Clinical Genomics Lab, St. Jude Children's Research Hospital: Collection method of the submission from St. Jude Clinical Genomics Lab, St. Jude Children's Research Hospital:
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
NM_000551.4(VHL):c.241C>T (p.Pro81Ser) rs104893829

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