ClinVar Miner

Variants with conflicting interpretations "uncertain significance" from Baylor Genetics and "likely pathogenic" from PreventionGenetics, part of Exact Sciences

Minimum review status of the submission from Baylor Genetics: Collection method of the submission from Baylor Genetics:
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_002016.2(FLG):c.2282_2285del (p.Ser761fs) rs558269137

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