ClinVar Miner

Variants with conflicting interpretations "likely pathogenic" from Institute of Reproductive Genetics, University of Münster and "pathogenic" from any submitter

Minimum review status of the submission from Institute of Reproductive Genetics, University of Münster: Collection method of the submission from Institute of Reproductive Genetics, University of Münster:
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_002440.4(MSH4):c.2261C>T (p.Ser754Leu) rs377712900

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