Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs761341952
rs761341952
FANCA
T 0.700 GeneticVariation CLINVAR Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology. 24584348

2014
dbSNP: rs761341952
rs761341952
FANCA
T 0.700 GeneticVariation CLINVAR Origin, functional role, and clinical impact of Fanconi anemia FANCA mutations. 21273304

2011
dbSNP: rs761341952
rs761341952
FANCA
T 0.700 CausalMutation CLINVAR Origin, functional role, and clinical impact of Fanconi anemia FANCA mutations. 21273304

2011
dbSNP: rs761341952
rs761341952
FANCA
T 0.700 CausalMutation CLINVAR Validation of Fanconi anemia complementation Group A assignment using molecular analysis. 19367192

2009
dbSNP: rs761341952
rs761341952
FANCA
T 0.700 CausalMutation CLINVAR Spectrum of sequence variations in the FANCA gene: an International Fanconi Anemia Registry (IFAR) study. 15643609

2005
dbSNP: rs761341952
rs761341952
FANCA
T 0.700 CausalMutation CLINVAR Fanconi anemia in Ashkenazi Jews. 15516848

2004
dbSNP: rs761341952
rs761341952
FANCA
T 0.700 CausalMutation CLINVAR Sequence variation in the Fanconi anemia gene FAA. 9371798

1997
dbSNP: rs761341952
rs761341952
FANCA
T 0.700 GeneticVariation CLINVAR Sequence variation in the Fanconi anemia gene FAA. 9371798

1997