Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2072590
rs2072590
HAGLR ; HAGLROS
T 0.720 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. 20852632

2010
dbSNP: rs3814113
rs3814113 		T 0.720 GeneticVariation GWASDB The most significant SNP (rs3814113; P = 2.5 x 10(-17)) was genotyped in a further 2,670 ovarian cancer cases and 4,668 controls, confirming its association (combined data odds ratio (OR) = 0.82, 95% confidence interval (CI) 0.79-0.86, P(trend) = 5.1 x 10(-19)). 19648919

2009
dbSNP: rs2363956
rs2363956
ANKLE1
T 0.710 GeneticVariation GWASDB Common variants at 19p13 are associated with susceptibility to ovarian cancer. 20852633

2010
dbSNP: rs1064795649
rs1064795649
BRIP1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1243180
rs1243180
MLLT10
T 0.700 GeneticVariation GWASDB GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer. 23535730

2013
dbSNP: rs138213197
rs138213197
HOXB13
T 0.700 CausalMutation CLINVAR

dbSNP: rs80357438
rs80357438
BRCA1 ; NBR2
T 0.700 CausalMutation CLINVAR

dbSNP: rs80357669
rs80357669
BRCA1
T 0.700 CausalMutation CLINVAR

dbSNP: rs80358981
rs80358981
BRCA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs869312756
rs869312756
ATM
T 0.700 GeneticVariation CLINVAR

dbSNP: rs10088218
rs10088218
LINC00824
G 0.710 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. 20852632

2010
dbSNP: rs17879961
rs17879961
CHEK2
G 0.710 GeneticVariation CLINVAR

dbSNP: rs757210
rs757210
HNF1B
G 0.700 GeneticVariation GWASDB GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer. 23535730

2013
dbSNP: rs80357828
rs80357828
BRCA1
G 0.700 CausalMutation CLINVAR

dbSNP: rs80359477
rs80359477
BRCA2
G 0.700 CausalMutation CLINVAR

dbSNP: rs9303542
rs9303542
SKAP1
G 0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. 20852632

2010
dbSNP: rs2665390
rs2665390
TIPARP ; LOC107986148
C 0.710 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. 20852632

2010
dbSNP: rs118203998
rs118203998
PALB2
C 0.700 CausalMutation CLINVAR

dbSNP: rs34612342
rs34612342
MUTYH
C 0.700 CausalMutation CLINVAR

dbSNP: rs63750695
rs63750695
PMS2
C 0.700 CausalMutation CLINVAR

dbSNP: rs80357233
rs80357233
BRCA1
C 0.700 CausalMutation CLINVAR

dbSNP: rs869312774
rs869312774
PALB2
C 0.700 CausalMutation CLINVAR

dbSNP: rs55770810
rs55770810
BRCA1
A 0.800 CausalMutation CLINVAR

dbSNP: rs1801155
rs1801155
APC
A 0.720 SusceptibilityMutation CLINVAR

dbSNP: rs11782652
rs11782652
CHMP4C
A 0.700 GeneticVariation GWASDB GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer. 23535730

2013