ClinVar Miner

Variants with conflicting interpretations "uncertain significance" from ISCA site 17 and "likely benign" 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: 1
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HGVS dbSNP gnomAD frequency
GRCh38/hg38 4q13.2-13.3(chr4:68852530-69850009)x3

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