ClinVar Miner

Submissions for variant NM_020630.5(RET):c.-200A>G

gnomAD frequency: 0.77447  dbSNP: rs10900296
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000265906 SCV000483060 benign Multiple endocrine neoplasia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000320981 SCV000483061 benign Renal hypodysplasia/aplasia 1 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000375701 SCV000483062 benign Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000281211 SCV000483063 benign Hirschsprung Disease, Dominant 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001692084 SCV001909551 benign not provided 2018-06-24 criteria provided, single submitter clinical testing

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