ClinVar Miner

Variants with conflicting interpretations "likely benign" from SIB Swiss Institute of Bioinformatics and "benign" from CFTR-France

Minimum review status of the submission from SIB Swiss Institute of Bioinformatics: Collection method of the submission from SIB Swiss Institute of Bioinformatics:
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_000492.4(CFTR):c.443T>C (p.Ile148Thr) rs35516286 0.00083

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