ClinVar Miner

Submissions for variant NM_153638.4(PANK2):c.-11G>A

gnomAD frequency: 0.00179  dbSNP: rs71647826
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000365190 SCV000341686 benign not specified 2016-05-30 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000365814 SCV000483949 likely benign Pigmentary pallidal degeneration 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV000675586 SCV001888276 benign not provided 2018-09-05 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000675586 SCV000801277 benign not provided 2018-02-14 no assertion criteria provided clinical testing

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