Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs41293459
rs41293459
BRCA1
0.020 GeneticVariation BEFREE We previously showed that variant BRCA1 c.5096G>A p.Arg1699Gln in the BRCA1 transcriptional transactivation domain demonstrated equivocal results from a series of functional assays, and proposed that this variant may confer low to moderate risk of cancer. 22889855

2012
dbSNP: rs41293459
rs41293459
BRCA1
0.020 GeneticVariation BEFREE We previously showed that variant BRCA1 c.5096G>A p.Arg1699Gln in the BRCA1 transcriptional transactivation domain demonstrated equivocal results from a series of functional assays, and proposed that this variant may confer low to moderate risk of cancer. 22889855

2012
dbSNP: rs41293459
rs41293459
BRCA1
0.020 GeneticVariation BEFREE The results also raise the possibility that A1708V and R1699Q may be associated with a low or moderate risk of cancer. 18036263

2007