ClinVar Miner

Variants with conflicting interpretations "pathogenic" from CFTR-France and "likely pathogenic" from CeGaT Center for Human Genetics Tuebingen

Minimum review status of the submission from CFTR-France: Collection method of the submission from CFTR-France:
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.3485G>T (p.Arg1162Leu) rs1800120

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