ClinVar Miner

Submissions for variant NM_000419.5(ITGA2B):c.1253del (p.Gly418fs)

dbSNP: rs2143465205
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001387239 SCV001587804 pathogenic Glanzmann thrombasthenia 2020-08-14 criteria provided, single submitter clinical testing Loss-of-function variants in ITGA2B are known to be pathogenic (PMID: 21917754). For these reasons, this variant has been classified as Pathogenic. This variant has not been reported in the literature in individuals with ITGA2B-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Gly418Alafs*13) in the ITGA2B gene. It is expected to result in an absent or disrupted protein product.

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