Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1805192
rs1805192
PPARG
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.050 GeneticVariation BEFREE The minor allele of rs1800206 and rs1805192 and its interaction were associated with increased BC risk. 28669518

2017
dbSNP: rs1805192
rs1805192
PPARG
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.050 GeneticVariation BEFREE Pro 12Ala and Ala203Pro polymorphisms did not modify the association between the iAs methylation capacity and BC. 27557380

2016
dbSNP: rs1805192
rs1805192
PPARG
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.050 GeneticVariation BEFREE The association between mono-(2-ethyl-5-hydroxyhexyl) phthalate (MEHHP) and BC risk was positively modified in PPARγ Pro12Ala C carriers. 23866026

2013
dbSNP: rs1805192
rs1805192
PPARG
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.050 GeneticVariation BEFREE A marginally significant increased risk of breast cancer was observed among women homozygous for the Ala allele of PPARgamma Pro12Ala. 17348446

2007
dbSNP: rs1805192
rs1805192
PPARG
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.050 GeneticVariation BEFREE No significant association was observed between PPARgamma Pro12Ala polymorphism and either incident breast cancer (odds ratio = 1.08, 95% confidence interval = 0.85-1.38 for Ala allele carriers compared to non-carriers), plasma hormones, plasma cholesterol, BMI, weight gain since age 18 years or waist-to-hip ratio. 12439219

2002