Variant: rs7940310 

    present in Gene: PAFAH1B2
    present in Chromosome: 11
    Position on Chromosome: 117153765
    Alleles of this Variant: T/A;C

rs7940310 in PAFAH1B2 gene and Protein measurement PMID 23696881 2013 Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation.

rs7940310 in PAFAH1B2 gene and Soluble Transferrin Receptor Measurement PMID 23696881 2013 Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation.

rs7940310 in PAFAH1B2 gene and Triglycerides measurement PMID 23063622 2012 Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.