ClinVar Miner

Submissions for variant NM_020975.6(RET):c.*368G>T

dbSNP: rs756051983
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000390066 SCV000362412 uncertain significance Hirschsprung Disease, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000312483 SCV000362413 uncertain significance Renal hypodysplasia/aplasia 1 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000369487 SCV000362414 uncertain significance Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000269418 SCV000362415 uncertain significance Multiple endocrine neoplasia 2016-06-14 criteria provided, single submitter clinical testing

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