ClinVar Miner

Variants with conflicting interpretations "pathogenic" from Research and Development,Genoox and "likely pathogenic" from any submitter

Minimum review status of the submission from Research and Development,Genoox: Collection method of the submission from Research and Development,Genoox:
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
NM_000051.3(ATM):c.2921+1G>A rs587781558

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