ClinVar Miner

Variants with conflicting interpretations "likely pathogenic" from Department of Genetic, Henri Mondor Hospital,Assistance Publique des Hôpitaux de Paris and "uncertain significance" from Illumina Clinical Services Laboratory,Illumina

Minimum review status of the submission from Department of Genetic, Henri Mondor Hospital,Assistance Publique des Hôpitaux de Paris: Collection method of the submission from Department of Genetic, Henri Mondor Hospital,Assistance Publique des Hôpitaux de Paris:
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_003126.4(SPTA1):c.6421C>T (p.Arg2141Trp) rs41273519

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