Variant: rs217181 

    present in Gene: TXNL4B
    present in Chromosome: 16
    Position on Chromosome: 72080103
    Alleles of this Variant: C/T

rs217181 in TXNL4B gene and Blood Protein Measurement PMID 29875488 2018 Genomic atlas of the human plasma proteome.

rs217181 in TXNL4B gene and Calcification of coronary artery PMID 22916037 2012 Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.

rs217181 in TXNL4B gene and Ferritin measurement PMID 28240269 2017 Connecting genetic risk to disease end points through the human blood plasma proteome.

rs217181 in TXNL4B gene and Serum albumin measurement PMID 22286219 2012 Genome-wide association study identifies multiple loci influencing human serum metabolite levels.

rs217181 in TXNL4B gene and Serum ferritin measurement PMID 28240269 2017 Connecting genetic risk to disease end points through the human blood plasma proteome.

rs217181 in TXNL4B gene and Serum total cholesterol measurement PMID 23063622 2012 Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.