ClinVar Miner

Variants with conflicting interpretations "likely pathogenic" from Center for Individualized Medicine,Mayo Clinic and "pathogenic" from any submitter

Minimum review status of the submission from Center for Individualized Medicine,Mayo Clinic: Collection method of the submission from Center for Individualized Medicine,Mayo Clinic:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 4
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HGVS dbSNP
NM_000051.3(ATM):c.4111delG rs797045114
NM_000135.4(FANCA):c.4015del (p.Leu1339fs) rs762902309
NM_000553.6(WRN):c.487_488del (p.Asp163fs) rs797045118
NM_001113378.2(FANCI):c.2422A>T rs375656231

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