rs1590173934
This variant is located in the PNPLA2 gene.
▶ClinVar annotation
About PNPLA2
This gene encodes an enzyme which catalyzes the first step in the hydrolysis of triglycerides in adipose tissue. Mutations in this gene are associated with neutral lipid storage disease with myopathy. [provided by RefSeq, Jul 2010]
View all PNPLA2 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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