Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs986710868
rs986710868
FANCA ; ZNF276
C 0.700 GeneticVariation CLINVAR Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia. 23613520

2013
dbSNP: rs986710868
rs986710868
FANCA ; ZNF276
T 0.700 GeneticVariation CLINVAR Sequence variation in the Fanconi anemia gene FAA. 9371798

1997