Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs370228071
rs370228071
RAD51D ; RAD51L3-RFFL
0.010 GeneticVariation BEFREE Using deep sequencing and case-control genotyping studies, we show that in French Canadians, the missense <i>RAD51D</i> variant c.620C>T;p.S207L is highly prevalent and is associated with a significantly increased risk for ovarian high-grade serous carcinoma (HGSC; 3.8% cases vs. 0.2% controls). 28646019

2017