ClinVar Miner

Submissions for variant NM_004519.4(KCNQ3):c.-148_-147insTG

dbSNP: rs886062698
Minimum review status: Collection method:
Minimum conflict level:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breakthrough Genomics, Breakthrough Genomics RCV002292442 SCV005196112 uncertain significance not provided criteria provided, single submitter not provided
CeGaT Center for Human Genetics Tuebingen RCV002292442 SCV002586244 benign not provided 2023-03-01 criteria provided, single submitter clinical testing KCNQ3: BS1, BS2

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