Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs62514004
rs62514004
Entrez Id: 8840
Gene Symbol: CCN4
CCN4
CUI: C0027651
Disease:
Neoplasms
0.010 GeneticVariation BEFREE Patients carrying the WISP1 rs2929973 GG + TT variant were almost twice as likely as those carrying the GT genotype to have estrogen receptor (ER)- and progesterone receptor (PR)-positive tumors, while those with the WISP1 rs62514004 AG + GG genetic variants were around twice as likely as those with the AA genotype to have HER2-positive tumors. 31689877 2019