ClinVar Miner

Submissions for variant NM_001355436.2(SPTB):c.2656G>T (p.Val886Leu)

dbSNP: rs146031194
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000313348 SCV000387803 uncertain significance Elliptocytosis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000368002 SCV000387804 uncertain significance Spherocytosis, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002520909 SCV003282276 likely benign not provided 2024-03-13 criteria provided, single submitter clinical testing

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