Variant: rs2287997

present in Gene: DHX38 present in Chromosome: 16 Position on Chromosome: 72106654 Alleles of this Variant: G/A

rs2287997 in DHX38 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.

rs2287997 in DHX38 gene and Serum albumin measurement PMID 22286219 2012 Genome-wide association study identifies multiple loci influencing human serum metabolite levels.