Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs149616199
rs149616199
FANCG
G 0.700 CausalMutation CLINVAR Diagnosis of Fanconi Anemia: Mutation Analysis by Multiplex Ligation-Dependent Probe Amplification and PCR-Based Sanger Sequencing. 22778927

2012
dbSNP: rs149616199
rs149616199
FANCG
G 0.700 CausalMutation CLINVAR Spectrum of sequence variation in the FANCG gene: an International Fanconi Anemia Registry (IFAR) study. 12552564

2003
dbSNP: rs149616199
rs149616199
FANCG
G 0.700 CausalMutation CLINVAR The Fanconi anaemia group G gene FANCG is identical with XRCC9. 9806548

1998