Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1801155
rs1801155
APC
A 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs397507802
rs397507802
BRCA2
TA 0.700 CausalMutation CLINVAR

dbSNP: rs570278423
rs570278423
SDHB
T 0.700 GeneticVariation CLINVAR

dbSNP: rs587781299
rs587781299
ATM ; C11orf65
TA 0.700 CausalMutation CLINVAR

dbSNP: rs62625284
rs62625284
PALB2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs80359604
rs80359604
BRCA2
C 0.700 CausalMutation CLINVAR

dbSNP: rs869312772
rs869312772
PALB2
A 0.700 CausalMutation CLINVAR

dbSNP: rs869312782
rs869312782
TP53
A 0.700 CausalMutation CLINVAR

dbSNP: rs1801516
rs1801516
ATM
0.020 GeneticVariation BEFREE Our results do not support association of the 5557G>A or ivs38-8T>C variant with increased breast cancer risk or with bilateral breast cancer. 16914028

2006
dbSNP: rs1801516
rs1801516
ATM
0.020 GeneticVariation BEFREE We discovered that the combination of 5557G-->A in cis position with IVS38-8 T-->C was associated with bilateral breast cancer (OR = 10.2; 95% CI = 3.1-33.8; p = 0.001). 15756685

2005
dbSNP: rs75023630
rs75023630
PALB2
0.010 GeneticVariation BEFREE The mutations p.Y743* and p.D498Y were identified in two familial patients diagnosed with unilateral or synchronous bilateral breast cancer at the ages of 29 and 39, respectively. 30309218

2019
dbSNP: rs1064794662
rs1064794662
BRCA1
0.010 GeneticVariation BEFREE Regarding the genotype-phenotype relation, mutation c.212 + 1G > A appeared in an important percentage of breast and ovarian cancer cases, c.5123C > A in bilateral breast cancer and c.9117G > A in bilateral breast cancer and ovarian cancer. 28477318

2017
dbSNP: rs80357287
rs80357287
BRCA1 ; NBR2
0.010 GeneticVariation BEFREE Regarding the genotype-phenotype relation, mutation c.212 + 1G > A appeared in an important percentage of breast and ovarian cancer cases, c.5123C > A in bilateral breast cancer and c.9117G > A in bilateral breast cancer and ovarian cancer. 28477318

2017
dbSNP: rs863224464
rs863224464
BRCA2
0.010 GeneticVariation BEFREE Regarding the genotype-phenotype relation, mutation c.212 + 1G > A appeared in an important percentage of breast and ovarian cancer cases, c.5123C > A in bilateral breast cancer and c.9117G > A in bilateral breast cancer and ovarian cancer. 28477318

2017
dbSNP: rs879255477
rs879255477
BRCA1
0.010 GeneticVariation BEFREE Regarding the genotype-phenotype relation, mutation c.212 + 1G > A appeared in an important percentage of breast and ovarian cancer cases, c.5123C > A in bilateral breast cancer and c.9117G > A in bilateral breast cancer and ovarian cancer. 28477318

2017
dbSNP: rs149726976
rs149726976
GALNT12
0.010 GeneticVariation BEFREE In case of R297W-GALNT12, prediction of highly deleterious effect and disruption in ionic interactions were anticipated with reduction in enzymatic activity, associated with bilateral breast cancer and primary colorectal cancers. 24038392

2014
dbSNP: rs1800054
rs1800054
ATM
0.010 GeneticVariation BEFREE The subgroup of patients with bilateral breast carcinoma had a Ser49Cys frequency of 11.8% (2 of 17 patients), which again was significantly different from what was observed in the control group (P=0.024; Fisher two-sided exact test). 15042666

2004
dbSNP: rs28904921
rs28904921
ATM ; C11orf65
0.010 GeneticVariation BEFREE ATM variants 7271T>G and IVS10-6T>G among women with unilateral and bilateral breast cancer. 14562025

2003