ClinVar Miner

Variants with conflicting interpretations "likely pathogenic" from Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard and "pathogenic" from Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard

Minimum review status of the submission from Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard: Collection method of the submission from Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard:
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 gnomAD frequency
NM_003560.4(PLA2G6):c.1186+1G>A rs761815070

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