Variant: rs181929163

present in Gene: CEP112 present in Chromosome: 17 Position on Chromosome: 65744427 Alleles of this Variant: T/C

rs181929163 in CEP112 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.