ClinVar Miner

Variants with conflicting interpretations "likely risk allele" from HLA Laboratory, Instituto Nacional de Enfermedades Respiratorias Ismael Cosio Villegas and "benign" from GeneDx

Minimum review status of the submission from HLA Laboratory, Instituto Nacional de Enfermedades Respiratorias Ismael Cosio Villegas: Collection method of the submission from HLA Laboratory, Instituto Nacional de Enfermedades Respiratorias Ismael Cosio Villegas:
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_001001331.4(ATP2B2):c.1437C>T (p.Asn479=) rs2289274 0.26684

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