Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs752160950
rs752160950
FANCA
A 0.700 GeneticVariation CLINVAR DNA helicases FANCM and DDX11 are determinants of PARP inhibitor sensitivity. 25583207

2015
dbSNP: rs752160950
rs752160950
FANCA
A 0.700 GeneticVariation CLINVAR RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease. 25525159

2015
dbSNP: rs752160950
rs752160950
FANCA
A 0.700 GeneticVariation CLINVAR Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M. 19423727

2009
dbSNP: rs752160950
rs752160950
FANCA
A 0.700 GeneticVariation CLINVAR A rapid method for retrovirus-mediated identification of complementation groups in Fanconi anemia patients. 16084127

2005
dbSNP: rs752160950
rs752160950
FANCA
A 0.700 CausalMutation CLINVAR