rs1051931
This is a variant in the PLA2G7 gene that changes a valine to an alanine.
▶ClinVar annotation
Benign★☆☆☆
4 submitters2 publicationsPLA2G7-related disorder; RECLASSIFIED - PLA2G7 POLYMORPHISM
View on ClinVar →About PLA2G7
The protein encoded by this gene is a secreted enzyme that catalyzes the degradation of platelet-activating factor to biologically inactive products. Defects in this gene are a cause of platelet-activating factor acetylhydrolase deficiency. Two transcript variants encoding the same protein have been found for this gene.[provided by RefSeq, Dec 2009]
View all PLA2G7 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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