ClinVar Miner

Variants with conflicting interpretations "likely benign" from ISCA site 1 and "pathogenic" from Quest Diagnostics Nichols Institute San Juan Capistrano

Minimum review status of the submission from ISCA site 1: Collection method of the submission from ISCA site 1:
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
GRCh37/hg19 22q11.21(chr22:20716876-21465662)x1

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