ClinVar Miner

Variants with conflicting interpretations "likely pathogenic" from Eurofins NTD LLC (GA) and "likely benign" from Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

Minimum review status of the submission from Eurofins NTD LLC (GA): Collection method of the submission from Eurofins NTD LLC (GA):
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_000243.3(MEFV):c.1223G>A (p.Arg408Gln) rs11466024 0.01456

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