Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs334
rs334
HBB
A 0.850 CausalMutation CLINVAR Prevalence of the β(S) gene among scheduled castes, scheduled tribes and other backward class groups in Central India. 25023085

2014

dbSNP: rs334
rs334
HBB
A 0.850 CausalMutation CLINVAR The Prevalence of Sickle Cell Disease and Its Implication for Newborn Screening in Germany (Hamburg Metropolitan Area). 26275168

2016

dbSNP: rs334
rs334
HBB
A 0.850 CausalMutation CLINVAR Prevalence of sickle cell disease in a pediatric population suffering from severe infections: a Congolese experience. 25023084

2014

dbSNP: rs111645889
rs111645889
HBB
A 0.700 GeneticVariation CLINVAR

dbSNP: rs11549407
rs11549407
HBB
A 0.700 CausalMutation CLINVAR

dbSNP: rs33914668
rs33914668
HBB
C 0.700 CausalMutation CLINVAR

dbSNP: rs33915217
rs33915217
HBB
G 0.700 CausalMutation CLINVAR

dbSNP: rs33922842
rs33922842
HBB
A 0.700 CausalMutation CLINVAR

dbSNP: rs33930165
rs33930165
HBB
T 0.700 CausalMutation CLINVAR

dbSNP: rs33931746
rs33931746
HBB
G 0.700 CausalMutation CLINVAR

dbSNP: rs33931746
rs33931746
HBB
C 0.700 CausalMutation CLINVAR

dbSNP: rs33941377
rs33941377
HBB
T 0.700 CausalMutation CLINVAR

dbSNP: rs33941377
rs33941377
HBB
A 0.700 CausalMutation CLINVAR

dbSNP: rs33941849
rs33941849
HBB
C 0.700 CausalMutation CLINVAR

dbSNP: rs33944208
rs33944208
HBB
T 0.700 GeneticVariation CLINVAR

dbSNP: rs33945777
rs33945777
HBB
T 0.700 CausalMutation CLINVAR

dbSNP: rs33946267
rs33946267
HBB
T 0.700 CausalMutation CLINVAR

dbSNP: rs33946267
rs33946267
HBB
G 0.700 CausalMutation CLINVAR

dbSNP: rs33946267
rs33946267
HBB
A 0.700 CausalMutation CLINVAR

dbSNP: rs33947415
rs33947415
HBB
T 0.700 CausalMutation CLINVAR

dbSNP: rs33950507
rs33950507
HBB
T 0.700 CausalMutation CLINVAR

dbSNP: rs33951465
rs33951465
HBB
T 0.700 CausalMutation CLINVAR

dbSNP: rs33960103
rs33960103
HBB
G 0.700 CausalMutation CLINVAR

dbSNP: rs33971440
rs33971440
HBB
T 0.700 CausalMutation CLINVAR

dbSNP: rs33971440
rs33971440
HBB
A 0.700 CausalMutation CLINVAR