Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13689
rs13689
0.020 GeneticVariation BEFREE Four SNPs [rs3218550 (XRCC2), rs6917 (PHB), rs1801516 (ATM), and rs1368</span>9 (CDH1)] were significantly associated with risk of breast cancer. 29433565

2018

dbSNP: rs13689
rs13689
0.020 GeneticVariation BEFREE For survival analyses, the results demonstrated that the minor allele homozygotes of rs13689 and haplotype TGC in CDH1 were linked with unfavorable event-free survival of breast cancer, whereas, rs4783689 of CDH1 showed the opposite effect under dominant model. 26285011

2015

dbSNP: rs786202482
rs786202482
0.010 GeneticVariation BEFREE We also identified a likely damaging germline rs35352891 in the MUTYH gene (c.1118C>T, p.Ala373Val) in one Buryat Mongol BC patient. 31273614

2019

dbSNP: rs16260
rs16260
0.010 GeneticVariation BEFREE A significant association was found between TP53Arg72Pro (rs1042522) and CDH1 -160 C/A (rs16260) polymorphisms and breast cancer risk. 26666818

2016

dbSNP: rs12185157
rs12185157
0.010 GeneticVariation BEFREE For association analyses of germline variants with breast cancer susceptibility, the results showed that rs7200690, rs7198799, rs17715799, rs13689 and diplotype CGC/TGC (rs7200690 + rs12185157 + rs7198799) in CDH1 as well as rs2293303 in CTNNB1 were associated with increased breast cancer risk. 26285011

2015

dbSNP: rs17715799
rs17715799
0.010 GeneticVariation BEFREE For association analyses of germline variants with breast cancer susceptibility, the results showed that rs7200690, rs7198799, rs17715799</span>, rs13689 and diplotype CGC/TGC (rs7200690 + rs12185157 + rs7198799) in CDH1 as well as rs2293303 in CTNNB1 were associated with increased breast cancer risk. 26285011

2015

dbSNP: rs7198799
rs7198799
0.010 GeneticVariation BEFREE For association analyses of germline variants with breast cancer susceptibility, the results showed that rs7200690, rs7198799, rs17715799, rs13689 and diplotype CGC/TGC (rs7200690 + rs12185157 + rs7198799) in CDH1 as well as rs2293303 in CTNNB1 were associated with increased breast cancer risk. 26285011

2015

dbSNP: rs7200690
rs7200690
0.010 GeneticVariation BEFREE For association analyses of germline variants with breast cancer susceptibility, the results showed that rs7200690, rs7198799, rs17715799, rs13689 and diplotype CGC/TGC (rs7200690 + rs12185157 + rs7198799) in CDH1 as well as rs2293303 in CTNNB1 were associated with increased breast cancer risk. 26285011

2015