ClinVar Miner

Variants with conflicting interpretations "benign" from GeneDx and "uncertain significance" from Natera, Inc.

Minimum review status of the submission from GeneDx: Collection method of the submission from GeneDx:
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_001142800.2(EYS):c.977G>A (p.Ser326Asn) rs112822256 0.00379

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