Variant: rs142143628

present in Gene: CLVS1;LOC100130298 present in Chromosome: 8 Position on Chromosome: 60967385 Alleles of this Variant: C/T

rs142143628 in CLVS1;LOC100130298 gene and Venous Thromboembolism PMID 28203683 2017 Among 393 AA VTE cases and 4,941 AA controls, three intragenic SNPs reached genome-wide significance: LEMD3 rs138916004 (OR=3.2; p=1.3E-08), LY86 rs3804476 (OR=1.8; p=2E-08) and LOC100130298 rs142143628 (OR=4.5; p=4.4E-08); all three SNPs validated using internal cross-validation, parametric bootstrap and meta-analysis methods.