Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397509035
rs397509035
BRCA1
C 0.700 CausalMutation CLINVAR Prevalence and spectrum of BRCA germline variants in mainland Chinese familial breast and ovarian cancer patients. 26848529

2016
dbSNP: rs397509035
rs397509035
BRCA1
C 0.700 CausalMutation CLINVAR The prevalence of BRCA1 and BRCA2 germline mutations in high-risk breast cancer patients of Chinese Han nationality: two recurrent mutations were identified. 17851763

2008
dbSNP: rs397509035
rs397509035
BRCA1
C 0.700 CausalMutation CLINVAR Phosphorylation states of cell cycle and DNA repair proteins can be altered by the nsSNPs. 16111488

2005