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 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 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 Prevalence of sickle cell disease in a pediatric population suffering from severe infections: a Congolese experience. 25023084

2014

dbSNP: rs334
rs334
HBB
0.850 GeneticVariation UNIPROT Structure of fully liganded Hb ζ2β2s trapped in a tense conformation. 24100324

2013

dbSNP: rs334
rs334
HBB
0.850 GeneticVariation UNIPROT How malaria has affected the human genome and what human genetics can teach us about malaria. 16001361

2005

dbSNP: rs334
rs334
HBB
0.850 GeneticVariation UNIPROT Crystal structure of sickle-cell deoxyhemoglobin at 5 A resolution. 1195378

1975

dbSNP: rs334
rs334
HBB
0.850 GeneticVariation UNIPROT Gene mutations in human haemoglobin: the chemical difference between normal and sickle cell haemoglobin. 13464827

1957

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