Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs35894115
rs35894115
HBB
AT 0.700 CausalMutation CLINVAR Hb S-β-thalassemia: molecular, hematological and clinical comparisons. 21250876

2011
dbSNP: rs35894115
rs35894115
HBB
AT 0.700 CausalMutation CLINVAR Hemoglobinopathies in North Africa: a review. 20113284

2010
dbSNP: rs35894115
rs35894115
HBB
AT 0.700 CausalMutation CLINVAR Molecular heterogeneity of beta-thalassemia in Algeria: how to face up to a major health problem. 19205970

2009
dbSNP: rs35894115
rs35894115
HBB
AT 0.700 CausalMutation CLINVAR Detection of two rare beta-thalassemia alleles found in the Tunisian population: codon 47 (+A) and codons 106/107 (+G). 16987798

2006
dbSNP: rs35894115
rs35894115
HBB
AT 0.700 CausalMutation CLINVAR A novel frameshift mutation [FSC 47 (+A)] causing beta-thalassemia in a Surinam patient. 2283303

1990
dbSNP: rs35894115
rs35894115
HBB
AT 0.700 CausalMutation CLINVAR Observations on the levels of Hb A2 in patients with different beta-thalassemia mutations and a delta chain variant. 1698102

1990
dbSNP: rs35894115
rs35894115
HBB
AT 0.700 CausalMutation CLINVAR Thalassemia minor associated with hemoglobin-B2 heterozygosity. A family report. 13716727

1961