ClinVar Miner

Variants with conflicting interpretations "benign" from IntelligeneCG and "uncertain significance" from any submitter

Minimum review status of the submission from IntelligeneCG: Collection method of the submission from IntelligeneCG:
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 gnomAD frequency
NM_000546.6(TP53):c.215C>G (p.Pro72Arg) rs1042522 0.62654

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