ClinVar Miner

Submissions for variant NM_007214.5(SEC63):c.1936-7_1936-5dup

gnomAD frequency: 0.15112  dbSNP: rs766716921
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000293420 SCV000459448 uncertain significance Polycystic liver disease 1 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000293420 SCV000459449 benign Polycystic liver disease 1 2016-06-14 criteria provided, single submitter clinical testing

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