ClinVar Miner

Variants with conflicting interpretations "uncertain significance" from St. Jude Clinical Genomics Lab, St. Jude Children's Research Hospital and "benign" from any submitter

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: 5
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HGVS dbSNP
NM_000321.2(RB1):c.731T>C (p.Ile244Thr) rs147754935
NM_000548.5(TSC2):c.5336A>G (p.Gln1779Arg) rs748947919
NM_020975.6(RET):c.1699G>A (p.Asp567Asn) rs147219360
NM_020975.6(RET):c.200G>A (p.Arg67His) rs192489011
NM_177438.2(DICER1):c.2720T>C (p.Ile907Thr) rs200408568

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