KLKB1, kallikrein B1, 3818

N. diseases: 88; N. variants: 63
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2102575
rs2102575
Entrez Id: 3818;285440
Gene Symbol: KLKB1;CYP4V2
KLKB1;CYP4V2
CUI: C1861172
Disease:
Venous Thromboembolism
0.700 GeneticVariation GWASDB A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q. 22672568 2012