ClinVar Miner

Variants with conflicting interpretations "uncertain significance" from St. Jude Clinical Genomics Lab, St. Jude Children's Research Hospital and "likely benign" from Quest Diagnostics Nichols Institute San Juan Capistrano

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: 2
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HGVS dbSNP
NM_006231.4(POLE):c.1337G>A (p.Arg446Gln) rs151273553
NM_020975.6(RET):c.3112A>G (p.Thr1038Ala) rs201740483

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