ClinVar Miner

Submissions for variant NM_005570.4(LMAN1):c.539+5GT[3]

dbSNP: rs3835325
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000246703 SCV000311116 benign not specified criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000283539 SCV000409830 likely benign Factor V and factor VIII, combined deficiency of, type 1 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001683053 SCV001902596 benign not provided 2021-06-19 criteria provided, single submitter clinical testing

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