ClinVar Miner

Variants with conflicting interpretations "benign" from ISCA site 17 and "uncertain significance" from any submitter

Minimum review status of the submission from ISCA site 17: Collection method of the submission from ISCA site 17:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 3
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HGVS dbSNP gnomAD frequency
GRCh38/hg38 15q11.2(chr15:22572809-23066575)x3
GRCh38/hg38 4q35.2(chr4:189111218-189975519)x1
GRCh38/hg38 9p24.3(chr9:204193-295405)x3

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