Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17879961
rs17879961
G 0.710 GeneticVariation CLINVAR

dbSNP: rs17879961
rs17879961
0.710 GeneticVariation BEFREE The association between the I157T missense variant was then confirmed in a second sample of Russian patients with borderline ovarian cancers</span> (OR = 2.7; P = 0.06). 16828850

2006