Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3809072
rs3809072
Entrez Id: 11145;107984336
Gene Symbol: PLAAT3;LOC107984336
PLAAT3;LOC107984336
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE Two haplotypes (CTC and GGA) of rs11600655, rs3809073 and rs3809072, were relevant to CRC risk. 30343388 2019