ClinVar Miner

Submissions for variant NM_005570.4(LMAN1):c.1228A>T (p.Met410Leu)

gnomAD frequency: 0.10604  dbSNP: rs2298711
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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 RCV000251037 SCV000311111 benign not specified criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000366036 SCV000409823 benign Factor V and factor VIII, combined deficiency of, type 1 2018-01-12 criteria provided, single submitter clinical testing This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score and internal cut-off values, a variant classified as benign is not then subjected to further curation. The score for this variant resulted in a classification of benign for this disease.
GeneDx RCV001689855 SCV001912581 benign not provided 2018-11-12 criteria provided, single submitter clinical testing

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